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Merck

147249

Sigma-Aldrich

庚酰氯

99%

别名:

庚酸氯, 正庚酰氯

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About This Item

线性分子式:
CH3(CH2)5COCl
CAS号:
分子量:
148.63
Beilstein:
605636
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

99%

表单

liquid

折射率

n20/D 1.43 (lit.)

沸点

173 °C (lit.)

密度

0.96 g/mL at 25 °C (lit.)

官能团

acyl chloride

SMILES字符串

CCCCCCC(Cl)=O

InChI

1S/C7H13ClO/c1-2-3-4-5-6-7(8)9/h2-6H2,1H3

InChI key

UCVODTZQZHMTPN-UHFFFAOYSA-N

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一般描述

在氯化锡存在下,庚酰氯与2-乙基噻吩反应,生成2-乙基-5-庚酰噻吩

应用

庚酰氯被用于合成5α二氢睾酮庚酸酯 和γ-酮醛。它被用于制备酯连接的双层薄膜

象形图

Skull and crossbonesCorrosion

警示用语:

Danger

危险声明

危险分类

Acute Tox. 1 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

闪点(°F)

154.4 °F - closed cup

闪点(°C)

68 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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New. gamma.-keto Aldehyde synthesis.
Stowell JCl.
The Journal of Organic Chemistry, 41(3), 560-561 (1976)
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Clinical chemistry, 43(11), 2091-2098 (1997-11-20)
A recommended confirmatory procedure for detecting 5 alpha-dihydrotestosterone (DHT) doping in male athletes proposed the use of the urinary concentration ratio of DHT to epitestosterone (EpiT) as the primary marker and those of 5 alpha-androstane-3 alpha,17 beta-diol (5 alpha-Adiol) to
R D English et al.
Analytical chemistry, 72(24), 5973-5980 (2001-01-05)
We show that selected self-assembled monolayers (SAMs) and bilayers are readily characterized by the application of controlled photooxidation and spontaneous desorption mass spectrometry (SDMS) in the negative ion mode. Additionally, SDMS is used to characterize organic and inorganic anionic species
Synthetical applications of the desulphurisation reaction. Part I. The synthesis of fatty acids.
Badger GM, et al.
Journal of the Chemical Society, 4162-4168 (1954)
Chih-Ying Chien et al.
Carbohydrate polymers, 155, 440-447 (2016-10-06)
Regioselectively substituted curdlan esters were synthesized by protecting the C6 primary hydroxyl group with a triphenylmethyl group followed by the acylation of the secondary hydroxyl groups at C2 and C4. The subsequent detritylation of C6 trityl group under acidic conditions

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