China Largest Manufacturer factory sales 3,5-Di-tert-butylsalicylaldehyde CAS 37942-07-7 CAS NO.37942-07-7

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3,5-Di-tert-butylsalicylaldehyde Basic information Product Name: 3,5-Di-tert-butylsalicylaldehyde Synonyms: 3,5- di Ding JishuiYang Quan;3,5-Di-tert-butylsalicylaldehyde, 95+%;3, 5-2 tertiary butyl salicylaldehyde;3,5-Di-tert-butylsalicylaldehyde;3,5-Di-tert-butyl-2-hydroxybenzaldehyde 99%;2-Hydroxy-3,5-di-tert-butylbenzaldehyde;3,5-DI-TBUTYLSALICYLALDEHYDE;3,5-DI-TERT-BUTYL-2-HYDROXYBENZALDEHYDE CAS: 37942-07-7 MF: C15H22O2 MW: 234.33 EINECS: 629-676-0 Product Categories: Building Blocks;C13-C60;Aromatic Aldehydes & Derivatives (substituted);Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Aldehydes;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het;Achiral Oxygen Mol File: 37942-07-7.mol   3,5-Di-tert-butylsalicylaldehyde Chemical Properties Melting point  59-61 °C(lit.) Boiling point  277.6±35.0 °C(Predicted) density  1.006±0.06 g/cm3(Predicted) storage temp.  Keep in dark place,Sealed in dry,Room Temperature solubility  Soluble in DMSO and methanol. pka 9.78±0.23(Predicted) form  Solid color  Off-White to Light Yellow Sensitive  Air Sensitive BRN  1877810 InChIKey RRIQVLZDOZPJTH-UHFFFAOYSA-N CAS DataBase Reference 37942-07-7(CAS DataBase Reference)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38 Safety Statements  26-36 WGK Germany  3 Hazard Note  Irritant HS Code  29124990 MSDS Information Provider Language SigmaAldrich English ALFA English   3,5-Di-tert-butylsalicylaldehyde Usage And Synthesis Chemical Properties 3,5-Di-tert-butylsalicylaldehyde is white to yellow powder or chunks or crystal or crystalline powder Uses 3,5-Di-tert-butylsalicylaldehyde is a salicylaldehyde derivative with antibacterial activity used in the preparation nickel complexes. 3,5-Di-tert-butylsalicylaldehyde is structurally related to 3,5-di-t-butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC). Uses 3,5-Di-tert-butyl-2-hydroxybenzaldehyde is used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose, chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenyl acetylene to imines, chiral oxazolidine ligand for the enantioselective addition of diethyl zinc to aldehydes and tin Schiff base complexes with histidine analogues. It has antibacterial activity and is used in the preparation nickel complexes. It is structurally related to 3,5-di-t-butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC). Uses 3,5-Di-tert-butyl-2-hydroxybenzaldehyde was used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenylacetylene to imines chiral oxazolidine ligand for the enantioselective addition of diethylzinc to aldehydes tin Schiff base complexes with histidine analogues Synthesis Reference(s) The Journal of Organic Chemistry, 59, p. 1939, 1994 DOI: 10.1021/jo00086a062 Tetrahedron, 46, p. 793, 1990 DOI: 10.1016/S0040-4020(01)81362-4 Tetrahedron Letters, 13, p. 4205, 1972 DOI: 10.1016/S0040-4039(01)94276-5 General Description 3,5-Di-tert-butyl-2-hydroxybenzaldehyde undergoes condensation reaction with methyl-2-{N-(2′-aminoethane)}-amino-1-cyclopentenedithiocarboxylate to yield Schiff base ligand N,N-diethyl-2-methyl-1,4-phenylenediamine during the synthesis of copper(II) and cobalt(II) complexes of salicylaldimine   3,5-Di-tert-butylsalicylaldehyde Preparation Products And Raw materials Preparation Products (R)-(+)-2-Methyl-2-propanesulfinamide-->1,4,7,10,13-PENTAOXA-16-AZACYCLOOCTADECANE-->(S,S)-(+)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE

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Leader Biochemical Group is a large leader incorporated industry manufacturers and suppliers of advanced refined raw materials From the year of 1996 when our factory was put into production to year of 2020, our group has successively invested in more than 52 factories with shares and subordinates.We focus on manufacture Pharm & chemicals, functional active ingredients, nutritional Ingredients, health care products, cosmetics, pharmaceutical and refined feed, oil, natural plant ingredients industries to provide top quality of GMP standards products.All the invested factories' product lines cover API and intermediates, vitamins, amino acids, plant extracts, daily chemical products, cosmetics raw materials, nutrition and health care products, food additives, feed additives, essential oil products, fine chemical products and agricultural chemical raw materials And flavors and fragrances. Especially in the field of vitamins, amino acids, pharmaceutical raw materials and cosmetic raw materials, we have more than 20 years of production and sales experience. All products meet the requirements of high international export standards and have been recognized by customers all over the world. Our manufacture basement & R&D center located in National Aerospace Economic & Technical Development Zone Xi`an Shaanxi China. Now not only relying on self-cultivation and development as well as maintains good cooperative relations with many famous research institutes and universities in China. Now, we have closely cooperation with Shanghai Institute of Organic Chemistry of Chinese Academy of Science, Beijing Institute of Material Medical of Chinese Academy of Medical Science, China Pharmaceutical University, Zhejiang University. Closely cooperation with them not only integrating Science and technology resources, but also increasing the R&D speed and improving our R&D power. Offering Powerful Tech supporting Platform for group development. Keep serve the manufacture and the market as the R&D central task, focus on the technical research.  Now there are 3 technology R & D platforms including biological extract, microorganism fermentation and chemical synthesis, and can independently research and develop kinds of difficult APIs and pharmaceutical intermediates. With the strong support of China State Institute of Pharmaceutical Industry (hereinafter short for CSIPI), earlier known as Shanghai Institute of Pharmaceutical Industry (SIPI), we have unique advantages in the R & D and industrialization of high-grade, precision and advanced products.  Now our Group technical force is abundant, existing staff more that 1000 people, senior professional and technical staff accounted for more than 50% of the total number of employees, including 15 PhD research and development personnel, 5 master′ S degree in technical and management personnel 9 people. We have advanced equipment like fermentation equipment and technology also extraction, isolation, purification, synthesis with rich production experience and strict quality control system, According to the GMP required, quickly transforming the R&D results to industrial production in time, it is our advantages and our products are exported to North and South America, Europe, Middle East, Africa, and other five continents and scale the forefront in the nation, won good international reputation.  We believe only good quality can bring good cooperation, quality is our key spirit during our production, we are warmly welcome clients and partner from all over the world contact us for everlasting cooperation, Leader will be your strong, sincere and reliable partner in China.

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3,5-Di-tert-butylsalicylaldehyde Basic information Product Name: 3,5-Di-tert-butylsalicylaldehyde Synonyms: 3,5- di Ding JishuiYang Quan;3,5-Di-tert-butylsalicylaldehyde, 95+%;3, 5-2 tertiary butyl salicylaldehyde;3,5-Di-tert-butylsalicylaldehyde;3,5-Di-tert-butyl-2-hydroxybenzaldehyde 99%;2-Hydroxy-3,5-di-tert-butylbenzaldehyde;3,5-DI-TBUTYLSALICYLALDEHYDE;3,5-DI-TERT-BUTYL-2-HYDROXYBENZALDEHYDE CAS: 37942-07-7 MF: C15H22O2 MW: 234.33 EINECS: 629-676-0 Product Categories: Building Blocks;C13-C60;Aromatic Aldehydes & Derivatives (substituted);Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Aldehydes;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het;Achiral Oxygen Mol File: 37942-07-7.mol   3,5-Di-tert-butylsalicylaldehyde Chemical Properties Melting point  59-61 °C(lit.) Boiling point  277.6±35.0 °C(Predicted) density  1.006±0.06 g/cm3(Predicted) storage temp.  Keep in dark place,Sealed in dry,Room Temperature solubility  Soluble in DMSO and methanol. pka 9.78±0.23(Predicted) form  Solid color  Off-White to Light Yellow Sensitive  Air Sensitive BRN  1877810 InChIKey RRIQVLZDOZPJTH-UHFFFAOYSA-N CAS DataBase Reference 37942-07-7(CAS DataBase Reference)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38 Safety Statements  26-36 WGK Germany  3 Hazard Note  Irritant HS Code  29124990 MSDS Information Provider Language SigmaAldrich English ALFA English   3,5-Di-tert-butylsalicylaldehyde Usage And Synthesis Chemical Properties 3,5-Di-tert-butylsalicylaldehyde is white to yellow powder or chunks or crystal or crystalline powder Uses 3,5-Di-tert-butylsalicylaldehyde is a salicylaldehyde derivative with antibacterial activity used in the preparation nickel complexes. 3,5-Di-tert-butylsalicylaldehyde is structurally related to 3,5-di-t-butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC). Uses 3,5-Di-tert-butyl-2-hydroxybenzaldehyde is used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose, chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenyl acetylene to imines, chiral oxazolidine ligand for the enantioselective addition of diethyl zinc to aldehydes and tin Schiff base complexes with histidine analogues. It has antibacterial activity and is used in the preparation nickel complexes. It is structurally related to 3,5-di-t-butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC). Uses 3,5-Di-tert-butyl-2-hydroxybenzaldehyde was used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-β-L-idofuranose chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenylacetylene to imines chiral oxazolidine ligand for the enantioselective addition of diethylzinc to aldehydes tin Schiff base complexes with histidine analogues Synthesis Reference(s) The Journal of Organic Chemistry, 59, p. 1939, 1994 DOI: 10.1021/jo00086a062 Tetrahedron, 46, p. 793, 1990 DOI: 10.1016/S0040-4020(01)81362-4 Tetrahedron Letters, 13, p. 4205, 1972 DOI: 10.1016/S0040-4039(01)94276-5 General Description 3,5-Di-tert-butyl-2-hydroxybenzaldehyde undergoes condensation reaction with methyl-2-{N-(2′-aminoethane)}-amino-1-cyclopentenedithiocarboxylate to yield Schiff base ligand N,N-diethyl-2-methyl-1,4-phenylenediamine during the synthesis of copper(II) and cobalt(II) complexes of salicylaldimine   3,5-Di-tert-butylsalicylaldehyde Preparation Products And Raw materials Preparation Products (R)-(+)-2-Methyl-2-propanesulfinamide-->1,4,7,10,13-PENTAOXA-16-AZACYCLOOCTADECANE-->(S,S)-(+)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE