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Coco Acid Chloride
Negotiable
Category: Chemicals/Chemical Intermediates/Intermediate Compounds
Company: Suzhou Wedo Chemicals Co., Ltd.
Product Description: CAS NO:68187-89-3EC NO:269-133-1Molecular Formula:Molecular Weight:Synonyms:;Coconut oil acid chlorides;Coconut oil fatty acid chloride;Coconut oil fatty acyl chloride;Coco Acid Chloride;Molecular Structure: more>
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2-Ethylhexanoyl Chloride
Negotiable
Category: Chemicals/Chemical Intermediates/Intermediate Compounds
Company: Suzhou Wedo Chemicals Co., Ltd.
Product Description: CAS NO:760-67-8EC NO:212-081-1Molecular Formula:C8H15ClOMolecular Weight:162.6571Synonyms:Hexanoyl chloride, 2-ethyl-;2-Ethylcaproyl chloride;2-Ethylhexanoic acid chloride;NSC 87892;(2R)-2-ethylhexanoyl chloride;(2S)-2-ethylhexanoyl chloride;Molecular Structure:CAS NO:760-67-8EC NO:212-081-1Molecular Formula:C8H15ClOMolecular Weight:162.6571Synonyms:Hexanoyl chloride, 2-ethyl-;2-Ethylcaproyl chloride;2-Ethylhexanoic acid chloride;NSC 87892;(2R)-2-ethylhexanoyl chloride;(2S)-2-ethylhexanoyl chloride;Molecular Structure: more>
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Iminodibenzyl carbonyl chloride
Negotiable
Category: Chemicals/Chemical Intermediates/Intermediate Compounds
Company: ChemFine International Co.,Ltd (CFI)
Product Description: CAS NO:33948-19-5EC NO:251-756-5Molecular Formula:C15H12ClNOMolecular Weight:257.7149Synonyms:;10,11-Dihydro-dibenz[b,f]azepine-5-carbonyl chloride;10,11-dihydro-5H-dibenzo[b,f]azepine-5-carbonyl chloride;Iminodibenzylcarbonyl chloride;iminodibenzyl carbonyl chloride;Molecular Structure: more>
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Trimethylacetyl chloride
$Negotiation
Category: Chemicals/Chemical Intermediates/Intermediate Compounds
Company: Tianjin Yuansu Chemical Reagent Co.,Limited
Product Description: Packing:50kg,200kg,250kg drum Specification:  CAS NO.:3282-30-2 Used mainly in used for synthesizing various antibiotics and drugs, including: Amoxicillin (Amoxicillin) Pesticide intermediates: used in the production of: Carbamate insecticides (such as imidacloprid) herbicides (such as isoxazolone and chlorfenapyr) Plant protection products such as insecticides and herbicides thirty-eight •Other uses:  Synthesis of peroxyesters (such as tert butyl peroxybutyrate) Monomers or modifiers in polymer polymerization Preparation of photosensitive materials and initiators (such as TBPP)   Synthesis lines: According to authoritative sources, the mainstream synthesis methods for trimethylacetyl chloride are as follows: 1. Trimethylacetic acid chlorination method (most commonly used) Raw material: trimethylacetic acid Chlorination agent: Thionyl chloride (SOCl ₂) Catalyst: Caprolactam (small amount) Reaction conditions: Heat to 70 ℃, first remove sulfoxide chloride by vacuum distillation, and then collect the 105 ℃fraction by atmospheric distillation Yield: Approximately 98% Reaction formula: (CH3) 3CCOOH+SOCl2 →(CH3) 3CCOCl+SO2+HCl (CH3) 3CCOOH+SOCl2 →(CH3) 3CCOCl+SO2+HCl 2. Other methods (less commonly used): Reaction of trimethylacetic acid with phosphorus trichloride (PCl ∝) Carbonylation of tert butyl chloride and carbon monoxide in the presence of a catalyst Isobutanol reacts with formic acid to produce trimethylacetic acid, which is then chlorinated more>
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