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359-14-8

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359-14-8 Usage

General Description

Chloroacetyl fluoride is a chemical compound with the formula C2H2ClFO. It is a colorless, highly flammable liquid with a pungent odor. Chloroacetyl fluoride is commonly used as an intermediate in the production of pharmaceuticals, pesticides, and other organic chemicals. It is also used as a reagent in organic synthesis reactions, particularly in the introduction of the acetyl group into various compounds. However, chloroacetyl fluoride is highly toxic and can be a severe irritant to the skin, eyes, and respiratory system. It should be handled with extreme caution and under strict safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 359-14-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 359-14:
(5*3)+(4*5)+(3*9)+(2*1)+(1*4)=68
68 % 10 = 8
So 359-14-8 is a valid CAS Registry Number.

359-14-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroacetyl fluoride

1.2 Other means of identification

Product number -
Other names Chlor-acetylfluorid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:359-14-8 SDS

359-14-8Downstream Products

359-14-8Relevant articles and documents

Nucleophilic Substitution Reactions at Chloro-Substituted Ozonides and at a Chlorinated Dimeric Peroxide

Griesbaum, Karl,Schlindwein, Konrad

, p. 8062 - 8066 (2007/10/03)

Reactions of substituted 3-chloro- (2a-4a) and 3,5-dichloro-1,2,4-trioxolanes (9a, 10a) with AgBF4 in the presence of LiF gave the corresponding fluoro-substituted ozonides (2b - 4b and 9b and 10b).Substitutions of some of these chlorinated ozonides by the methoxy and by the acetoxy groups, and of 3,6-dichloro-3,6-dimethyl-1,2,4,5-tetroxane (22a) with the acetoxy group have been achieved too.

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