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2,2-DI(ACETOXYMETHYL)PROPIONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17872-59-2

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17872-59-2 Usage

Type of compound

Acyl chloride derivative

Contains

Carbonyl group bonded to a chlorine atom

Usage

Reagent in organic synthesis to introduce propionyl group

Applications

Production of pharmaceuticals and agrochemicals, intermediate in synthesis of other organic compounds

Safety precautions

Corrosive and toxic, should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 17872-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17872-59:
(7*1)+(6*7)+(5*8)+(4*7)+(3*2)+(2*5)+(1*9)=142
142 % 10 = 2
So 17872-59-2 is a valid CAS Registry Number.

17872-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(acetyloxymethyl)-3-chloro-2-methyl-3-oxopropyl] acetate

1.2 Other means of identification

Product number -
Other names -

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:17872-59-2 SDS

17872-59-2Relevant academic research and scientific papers

A General Approach to Quaternary Center Construction from Couplings of Unactivated Alkenes and Acyl Xanthates

Jenkins, Ernest N.,Czaplyski, William L.,Alexanian, Erik J.

supporting information, p. 2350 - 2353 (2017/05/12)

A general, radical-mediated approach to quaternary center construction using unactivated alkenes as coupling partners is reported. In this strategy, acyl xanthates, readily accessed from carboxylic acids, serve as precursors to tertiary radicals. This strategy leverages the unique reactivity of xanthates to participate in efficient radical-mediated additions to unactivated alkenes, expanding the scope of quaternary center construction.

Synthesis, characterization, and 1H NMR self-diffusion studies of dendritic aliphatic polyesters based on 2,2-bis(hydroxymethyl)propionic acid and 1,1,1-tris(hydroxyphenyl)ethane

Ihre, Henrik,Hult, Anders,S?derlind, Erik

, p. 6388 - 6395 (2007/10/03)

Dendritic aliphatic polyesters of one, two, three, and four generations (M(w): 906, 1856, 3754, and 7549 g/mol) were synthesized in the convergent fashion, using 2,2-bis(hydroxymethyl)propionic acid as building block and 1,1,1-tris(hydroxyphenyl)ethane as

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