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82158-24-5

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82158-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82158-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,5 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82158-24:
(7*8)+(6*2)+(5*1)+(4*5)+(3*8)+(2*2)+(1*4)=125
125 % 10 = 5
So 82158-24-5 is a valid CAS Registry Number.

82158-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzofuran-2-yl-(2-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names -

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:82158-24-5 SDS

82158-24-5Downstream Products

82158-24-5Relevant articles and documents

Enantioselective reduction of benzofuranyl aryl ketones

Carpenter, Ian,Clarke, Matthew L.

supporting information; experimental part, p. 65 - 68 (2011/02/25)

Enantioselective transfer hydrogenation of benzofuranyl aryl ketones proceeds with moderate to good enantioselectivity even when the aryl group is not sterically differentiated by ortho-substituents. The best results are obtained with substrates that are functionalised by electron-withdrawing aryl groups that contrast with the electron-rich benzofuran, which is consistent with [Ru-ArC-H]·Ar π interactions acting as a control element. Enantioselective pressure hydrogenation gives lower enantioselectivity irrespective of electronic effects, unless the aryl group is ortho-substituted, in which case up to 86% ee can be realised. Georg Thieme Verlag Stuttgart - New York.

Palladium-catalysed Heteroannulation of Acetylenic Compounds: a Facile Method for the Synthesis of Benzofurans

Kundu, Nitya G.,Pal, Manojit,Mahanty, Jyan S.,Dasgupta, Swapan K.

, p. 41 - 42 (2007/10/02)

A convenient and general method for the synthesis of benzofurans from o-iodophenol and acetylenic compounds under palladium-catalysed conditions is described.

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