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1917-10-8

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1917-10-8 Usage

General Description

Vinyl 2-furoate, also known as 2-Furancarboxylic acid vinyl ester, is a chemical compound belonging to the family of vinyl esters. VINYL 2-FUROATE is used in the production of polymers and resins, where it acts as a reactive diluent or crosslinking agent. It is also used as a starting material in the synthesis of other organic compounds. Vinyl 2-furoate is known to have low toxicity, but its potential health effects have not been extensively studied. Overall, it is a versatile chemical that finds applications in various industries including adhesives, coatings, and plastics.

Check Digit Verification of cas no

The CAS Registry Mumber 1917-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1917-10:
(6*1)+(5*9)+(4*1)+(3*7)+(2*1)+(1*0)=78
78 % 10 = 8
So 1917-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O3/c1-2-9-7(8)6-4-3-5-10-6/h2-5H,1H2

1917-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name VINYL 2-FUROATE

1.2 Other means of identification

Product number -
Other names 2-Furancarbonsaeure-p-toluidid

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:1917-10-8 SDS

1917-10-8Downstream Products

1917-10-8Relevant articles and documents

-

Skvortsova et al.

, (1972)

-

Regio- and Stereoselective Chan-Lam-Evans Enol Esterification of Carboxylic Acids with Alkenylboroxines

Steemers, Luuk,Wijsman, Linda,van Maarseveen, Jan H.

supporting information, p. 4241 - 4245 (2018/10/02)

Efficient and scalable Cu(II)-mediated enol esterification methodology of carboxylic acids from alkenyl boroxines and boronic acids is presented. The reaction shows a wide scope in aliphatic and aromatic carboxylic acids in combination with several alkenyl boroxines. In the case of 2-substituted alkenyl boroxines the double bond configuration was fully retained in the enol ester product. Also N-hydroxyimides and imides could be transformed in the respective amidooxy vinyl enol ethers and vinyl enamides. Finally, with the exception of methionine, all other 19 canonical amino acids showed their compatibility to give the enol esters in a stereoselective fashion. (Figure presented.).

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