147249
庚酰氯
99%
别名:
庚酸氯, 正庚酰氯
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关于此项目
线性分子式:
CH3(CH2)5COCl
化学文摘社编号:
分子量:
148.63
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-775-3
Beilstein/REAXYS Number:
605636
MDL number:
产品名称
庚酰氯, 99%
InChI key
UCVODTZQZHMTPN-UHFFFAOYSA-N
InChI
1S/C7H13ClO/c1-2-3-4-5-6-7(8)9/h2-6H2,1H3
SMILES string
CCCCCCC(Cl)=O
assay
99%
form
liquid
refractive index
n20/D 1.43 (lit.)
bp
173 °C (lit.)
density
0.96 g/mL at 25 °C (lit.)
functional group
acyl chloride
Quality Level
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Application
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。
General description
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。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 1 Inhalation - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 1
flash_point_f
154.4 °F - closed cup
flash_point_c
68 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
New. gamma.-keto Aldehyde synthesis.
Stowell JCl.
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Chih-Ying Chien et al.
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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
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
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)
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