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山梨酸氯化物_分子结构_CAS_2614-88-2)
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山梨酸氯化物

产品号 688797 公司名称 Sigma Aldrich
CAS号 2614-88-2 公司网站 http://www.sigmaaldrich.com
分子式 C6H7ClO 电 话 1-800-521-8956
分子量 130.57218 传 真
纯 度 ≥80% 电子邮件
保 存 Chembase数据库ID: 141771

产品价格信息

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产品别名

标题
Sorbic chloride
IUPAC标准名
hexa-2,4-dienoyl chloride
IUPAC传统名
hexa-2,4-dienoyl chloride
别名
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

产品登记号

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

产品性质

危险公开号 34
安全公开号 26-36/37/39-45
德国WGK号 3
GHS危险品标识 GHS05
GHS警示词 Danger
GHS危险声明 H314
欧盟危险性物质标志 腐蚀性(Corrosive) 腐蚀性(Corrosive) (C)
MSDS下载 下载链接
个人保护装置 Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS警示性声明 P280-P305 + P351 + P338-P310
Empirical Formula (Hill Notation) C6H7ClO
纯度 ≥80%

产品详细信息

详细说明 (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
详细说明 (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

参考文献