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32521-09-8

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32521-09-8 Usage

Type of compound

Vinyl derivative of 1,3-dihydro-isobenzofuran (heterocyclic compound)

Usage

Organic synthesis, chemical industry, pharmaceutical and agrochemical applications

Reactivity

Ability to undergo various chemical reactions, versatile building block for complex organic molecule synthesis

Health and environmental risks

Consult safety data before handling

Applications

Organic synthesis, chemical industry, pharmaceutical and agrochemical applications

Chemical structure

Unique structure contributing to its potential use in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 32521-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,5,2 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32521-09:
(7*3)+(6*2)+(5*5)+(4*2)+(3*1)+(2*0)+(1*9)=78
78 % 10 = 8
So 32521-09-8 is a valid CAS Registry Number.

32521-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-1,3-dihydro-2-benzofuran

1.2 Other means of identification

Product number -
Other names 3-Vinyl-phthalan

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:32521-09-8 SDS

32521-09-8Downstream Products

32521-09-8Relevant articles and documents

Sequential hydrostannylation-cyclisation of δ- and ω-allenyl aryl halides. Cyclisation at the proximal carbon

Grigg, Ronald,Sansano, Jose M.

, p. 13441 - 13454 (2007/10/03)

Palladium catalysed hydrostannylation of (Bu3SnH, THF, O°C) of δ- and ω-allenyl aryl halides followed by mono- or bis-cyclisation (MeCN, 80°C) affords small (5-7), large (11-17) and spirocyclic rings in which cyclisation occurs at the proximal

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