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Sorbic chloride

Catalog No. 688797 Name Sigma Aldrich
CAS Number 2614-88-2 Website http://www.sigmaaldrich.com
M. F. C6H7ClO Telephone 1-800-521-8956
M. W. 130.57218 Fax
Purity ≥80% Email
Storage Chembase ID: 141771

SYNONYMS

Title
山梨酸氯化物
IUPAC name
hexa-2,4-dienoyl chloride
IUPAC Traditional name
hexa-2,4-dienoyl chloride
Synonyms
trans,trans-2,4-Hexadienoyl chloride
Sorboyl chloride
Sorbic acid chloride
trans,trans-Hexa-2,4-dienoyl chloride
(2E,4E)-2,4-Hexadienoyl chloride
(E,E)-2,4-Hexadienoyl chloride
反式,反式-2,4-己二烯酰氯
山梨酰氯

DATABASE IDS

CAS Number 2614-88-2
Beilstein Number 969473
MDL Number MFCD00045227

PROPERTIES

Risk Statements 34
Safety Statements 26-36/37/39-45
German water hazard class 3
GHS Pictograms GHS05
GHS Signal Word Danger
GHS Hazard statements H314
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Personal Protective Equipment Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P280-P305 + P351 + P338-P310
Empirical Formula (Hill Notation) C6H7ClO
Purity ≥80%

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of unsaturated hydroxymethylene diphosphonic acid derivatives by reaction of trimethylsilyl phosphites1
• Asymmetrical synthesis of the isoindolinone subunit of the macrocyclic poylketide natural product muironolide A via stereoselective intramolecular Diels-Alder cycloaddition2
• Preparation of emollient, humectant, and fluorescent α,β-unsaturated thiol esters for long-acting skin applications3
• Stereoselective synthesis of enediol carbonates for use in the asymmetrical synthesis of α-acyloxyketones4
• Acylation of pyrazoles5
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of unsaturated hydroxymethylene diphosphonic acid derivatives by reaction of trimethylsilyl phosphites1
• Asymmetrical synthesis of the isoindolinone subunit of the macrocyclic poylketide natural product muironolide A via stereoselective intramolecular Diels-Alder cycloaddition2
• Preparation of emollient, humectant, and fluorescent α,β-unsaturated thiol esters for long-acting skin applications3
• Stereoselective synthesis of enediol carbonates for use in the asymmetrical synthesis of α-acyloxyketones4
• Acylation of pyrazoles5

REFERENCES