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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:
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
hcodes
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
| SKU | GTIN |
|---|---|
| 147249-100G | 04061836682422 |
| 147249-25G | 04061838737298 |


