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重要文件

147249

Sigma-Aldrich

庚酰氯

99%

同義詞:

庚酸氯, 正庚酰氯

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About This Item

線性公式:
CH3(CH2)5COCl
CAS號碼:
分子量::
148.63
Beilstein:
605636
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

99%

形狀

liquid

折射率

n20/D 1.43 (lit.)

bp

173 °C (lit.)

密度

0.96 g/mL at 25 °C (lit.)

官能基

acyl chloride

SMILES 字串

CCCCCCC(Cl)=O

InChI

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

InChI 密鑰

UCVODTZQZHMTPN-UHFFFAOYSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

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

應用

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

象形圖

Skull and crossbonesCorrosion

訊號詞

Danger

危險聲明

危險分類

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

儲存類別代碼

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

水污染物質分類(WGK)

WGK 1

閃點(°F)

154.4 °F - closed cup

閃點(°C)

68 °C - closed cup

個人防護裝備

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


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New. gamma.-keto Aldehyde synthesis.
Stowell JCl.
The Journal of Organic Chemistry, 41(3), 560-561 (1976)
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
S B Coutts et al.
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
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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