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213617-52-8

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213617-52-8 Usage

Physical State

Yellow liquid

Usage

Production of pharmaceuticals, organic compounds, and flavoring agent in the food industry

Chemical Classification

Alpha,beta-unsaturated aldehyde

Toxicity

Can be toxic if ingested or inhaled

Chemical Structure

Contains a fluorophenyl group attached to a propenal chain

Applications

Used in research and industrial processes for its unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 213617-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,1 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213617-52:
(8*2)+(7*1)+(6*3)+(5*6)+(4*1)+(3*7)+(2*5)+(1*2)=108
108 % 10 = 8
So 213617-52-8 is a valid CAS Registry Number.

213617-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-fluorophenyl)acrylaldehyde

1.2 Other means of identification

Product number -
Other names (2Z)-3-(3-fluorophenyl)-2-propenal

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:213617-52-8 SDS

213617-52-8Downstream Products

213617-52-8Relevant articles and documents

Silicon-directed rhenium-catalyzed allylic carbaminations and oxidative fragmentations of γ-silyl allylic alcohols

Chavhan, Sanjay W.,Cook, Matthew J.

supporting information, p. 4891 - 4895 (2014/05/06)

A highly regioselective allylic substitution of β-silyl allylic alcohols has been achieved that provides the branched isomer as a single product. This high level of regiocontrol is achieved through the use of a vinyl silane group that can perform a Hiyama coupling providing 1,3-disubstituted allylic amines. An unusual oxidative fragmentation product was also observed at elevated temperature that appears to proceed by a Fleming-Tamao-type oxidation-elimination pathway.

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