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22577-15-7

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22577-15-7 Usage

Uses

3-Allyloxypropionic Acid is a useful intermediate for plasticizers and other chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 22577-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22577-15:
(7*2)+(6*2)+(5*5)+(4*7)+(3*7)+(2*1)+(1*5)=107
107 % 10 = 7
So 22577-15-7 is a valid CAS Registry Number.

22577-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-2-enoxypropanoic acid

1.2 Other means of identification

Product number -
Other names 3-Allyloxy-propionsaeure

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:22577-15-7 SDS

22577-15-7Relevant articles and documents

Preparation of 3-(n-alkenoxy)propanoic acids

Simonot,Rousseau

, p. 549 - 560 (1993)

3-(n-Alkenoxy)propanoic acids have been prepared by reaction of alkenols with tert-butyl acrylate (catalyzed by Triton B or n-butyl lithium) followed by cleavage of the tert-butyl group by CF3COOH or KO2.

Oxidative cyclization of alkenoic acids promoted by AgOAc

Carrillo-Arcos, Ulises A.,Rojas-Ocampo, Jonathan,Porcel, Susana

supporting information, p. 479 - 483 (2016/01/09)

Alkenoic acids derived from salicylic acid and analogues undergo an unexpected oxidative cyclization process triggered by AgOAc leading to 4H-benzo[d][1,3]dioxin-4-ones. The process is affected by the substitution on the aryl and the allyl units.

Kinetics of the Coupling Reactions of the Nitroxyl Radical 1,1,3,3-Tetramethylisoindoline-2-oxyl with Carbon-Centered Radicals

Beckwith, Athelstan L. J.,Bowry, Vincent W.,Moad, Graeme

, p. 1632 - 1641 (2007/10/02)

Radical clocks have been used to study the kinetics of the coupling of the nitroxyl radical 1,1,3,3-tetramethylisoindoline-2-oxyl (T) in cyclohexane or benzene with a variety of carbon-centered radicals including simple unhindered primary, secondary, and

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