C116807
Cyclopropanecarbonyl chloride
98%
Synonym(s):
Cyclopropanecarboxylic acid chloride
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About This Item
Linear Formula:
C3H5COCl
CAS Number:
Molecular Weight:
104.53
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-684-4
Beilstein/REAXYS Number:
471286
MDL number:
Assay:
98%
Form:
liquid
InChI
1S/C4H5ClO/c5-4(6)3-1-2-3/h3H,1-2H2
InChI key
ZOOSILUVXHVRJE-UHFFFAOYSA-N
SMILES string
ClC(=O)C1CC1
assay
98%
form
liquid
refractive index
n20/D 1.452 (lit.)
bp
119 °C (lit.)
density
1.152 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
Cyclopropanecarbonyl chloride can be used as an alkylating reagent in the preparation of some chemical building blocks such as formylcyclopropane, cyclopropanecarboxylic acid hydrazide, bis(cyclopropylcarbonyl) peroxide, 1-cyclopropanecarboxamide, 2-cyclopropylcarbonylcyclohexane-1,3-diones and cyclopropyl analog of triazolopiperazine-amides.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Reductive Oxidation of Acid Chlorides to Aldehydes with Sodium Borohydride and Pyridinium Chlorochromate
Cha JS and Lee DY
Bull. Korean Chem. Soc., 21(12), 1260-1262 (2000)
Yi Liu et al.
Journal of environmental sciences (China), 90, 180-188 (2020-02-23)
A novel N,N-dithenoyl-rhodamine based fluorescent and colorimetric Fe3+ probe 1 was designed and synthesized by only one step from Rhodamine B hydrazide and 2-thiophenecarbonyl chloride. The structure of probe 1 was characterized by 1H NMR/13C NMR spectroscopy, IR spectroscopy, and
Triazolopiperazine-amides as dipeptidyl peptidase IV inhibitors: Close analogs of JANUVIA?(sitagliptin phosphate)
Kim, Dooseop, et al.
Bioorganic & Medicinal Chemistry Letters, 17(12), 3373-3377 (2007)
Preparation of Pivaloyl Hydrazide in Water: (Propanoic acid, 2, 2-dimethyl-, hydrazide)
Li Bryan, et al.
Organic Syntheses, 81(23), 254-261 (2003)
Enzyme inhibition potency enhancement by active site metal chelating and hydrogen bonding induced conformation-restricted cyclopropanecarbonyl derivatives
Kuo P-Y, et al.
Bioorganic & Medicinal Chemistry Letters, 16(23), 6024-6027 (2006)
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