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Benzofuran, 3-[(phenylmethyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88673-96-5

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88673-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88673-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,7 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88673-96:
(7*8)+(6*8)+(5*6)+(4*7)+(3*3)+(2*9)+(1*6)=195
195 % 10 = 5
So 88673-96-5 is a valid CAS Registry Number.

88673-96-5SDS

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-benzylsulfanyl-1-benzofuran

1.2 Other means of identification

Product number -
Other names Benzofuran,3-[(phenylmethyl)thio]

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:88673-96-5 SDS

88673-96-5Downstream Products

88673-96-5Relevant academic research and scientific papers

Formation of Uncondensed Binuclear Heterocyclic Compounds in the Thio-Claisen Rearrangement of Heteroaromatic Sulfides

Anisimov, A. V.,Panov, S. M.,Sizoi, V. F.,Nepogod'ev, S. A.,Viktorova, E. A.

, p. 1072 - 1075 (1983)

Allyl hetaryl sulfides with an allyl fragment that is part of a heteroaromatic ring undergo a -sigmatropic rearrangement when they are heated in various solvents, as a result of which uncondensed binuclear heterocyclic compounds are formed.On the basis of kinetic data it was shown that the inclusion of the vinyl or allyl fragment of a sulfide in the composition of the heteroaromatic ring hinders the rearrangement more, the higher the aromatic character of the heteroring.

Regioselective synthesis of benzofuran-annulated six-membered sulfur heterocycles by aryl radical cyclization

Majumdar,Chattopadhyay,Nath

, p. 2907 - 2915 (2008/02/11)

The tin hydride-mediated cyclization of a number of sulfides and sulfones under mild and neutral conditions has been investigated. The sulfides were in turn derived from 3(2H) benzothiofuranone and 2-bromobenzyl bromides by phase-transfer-catalyzed reacti

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