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Merck
CN

147249

Heptanoyl chloride

99%

Synonym(s):

Enanthic chloride, Oenanthic chloride

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About This Item

Linear Formula:
CH3(CH2)5COCl
CAS Number:
Molecular Weight:
148.63
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-775-3
Beilstein/REAXYS Number:
605636
MDL number:
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Quality Level

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

SMILES string

CCCCCCC(Cl)=O

InChI

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

InChI key

UCVODTZQZHMTPN-UHFFFAOYSA-N

General description

Heptanoyl chloride reacts with 2-ethylthiophene in the presence of stannic chloride to give 2-ethyl-5-heptanoylthiophene.

Application

Heptanoyl chloride was used in synthesis of 5α-dihydrotestosterone heptanoate and γ-ketoaldehyde. It was used in the preparation of ester-linked bilayer films.


signalword

Danger

wgk

WGK 1

ppe

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

Hazard Classifications

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

Storage Class

3 - Flammable liquids

flash_point_f

116.6 °F - closed cup

flash_point_c

47 °C - closed cup



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



Global Trade Item Number

SKUGTIN
147249-100G04061836682422
147249-25G04061838737298