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Benzene, 1-[bis(methylseleno)methyl]-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105824-46-2

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105824-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105824-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105824-46:
(8*1)+(7*0)+(6*5)+(5*8)+(4*2)+(3*4)+(2*4)+(1*6)=112
112 % 10 = 2
So 105824-46-2 is a valid CAS Registry Number.

105824-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxyphenyl-bis(methylseleno)methane

1.2 Other means of identification

Product number -
Other names 1-(Bis-methylselanyl-methyl)-4-methoxy-benzene

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:105824-46-2 SDS

105824-46-2Relevant academic research and scientific papers

Regioselective syntheses of polycyclic compounds by carbanion-mediated polycyclisation of olefins

Krief,Barbeaux

, p. 417 - 420 (2007/10/02)

This paper reports straightforward syntheses of 1-aryl-bicyclo-[n. 1.0]-alkanes, 1-aryl-bicyclo-[3.3.0]-alkanes and of 1-phenyl-1,4-dimethyl-cyclopentane from unsaturated benzylselenides which involve the organolithiums-mediated cyclisation of olefins and

METALLATION OF BENZYL SELENIDES AND OF α-ARYL SELENOACETALS. SCOPE AND LIMITATIONS.

Clarembeau, M.,Krief, A.

, p. 1723 - 1726 (2007/10/02)

α-Metallo benzylselenides and α-metallo selenoacetals derived from aromatic aldehydes have been conveniently prepared by metallation of the corresponding carbon acids.KDA in THF proved among the various basic systems tested, the most efficient.

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