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3-Benzofuranmethanol, 2-ethyl-a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101596-60-5

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101596-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101596-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,9 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101596-60:
(8*1)+(7*0)+(6*1)+(5*5)+(4*9)+(3*6)+(2*6)+(1*0)=105
105 % 10 = 5
So 101596-60-5 is a valid CAS Registry Number.

101596-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-ethyl-benzofuran-3-yl)-phenyl-methanol

1.2 Other means of identification

Product number -
Other names (2-Ethyl-benzofuran-3-yl)-phenyl-methanol

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:101596-60-5 SDS

101596-60-5Downstream Products

101596-60-5Relevant academic research and scientific papers

Substituted oxadiazolidinediones

-

Page/Page column 11, (2010/02/11)

The present invention relates generally to substituted oxadiazolidinediones and methods of using them.

A New Preparation of Benzofurans Utilizing Trimethylsilyldiazomethane

Ito, Yasuko,Aoyama, Toyohiko,Shioiri, Takayuki

, p. 1163 - 1164 (2007/10/03)

o-Triisopropylsiloxyaryl ketones and aldehydes smoothly reacted with the lithium salt of trimethylsilyldiazomethane to give o-triisopropylsiloxyphenylacetylenes which were easily converted to benzofurans by treatment with tetra-n-butylammonium fluoride. 3-Benzofuranmethanols were also obtained when the reaction was conducted in the presence of carbonyl compounds.

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