Skip to Content
Merck
All Photos(2)

Documents

C116807

Sigma-Aldrich

Cyclopropanecarbonyl chloride

98%

Synonym(s):

Cyclopropanecarboxylic acid chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C3H5COCl
CAS Number:
4023-34-1
Molecular Weight:
104.53
Beilstein:
471286
EC Number:
223-684-4
MDL number:
MFCD00001277
UNSPSC Code:
12352100
PubChem Substance ID:
24892371
NACRES:
NA.22

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

SMILES string

ClC(=O)C1CC1

InChI

1S/C4H5ClO/c5-4(6)3-1-2-3/h3H,1-2H2

InChI key

ZOOSILUVXHVRJE-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

Signal Word

Danger

Hazard Statements

H226,H301,H314

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
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)
Preparation of Pivaloyl Hydrazide in Water: (Propanoic acid, 2, 2-dimethyl-, hydrazide)
Li Bryan, et al.
Organic Syntheses, 81(23), 254-261 (2003)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service