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Benzeneethanol, b-methyl-a-phenyl-b-(phenylseleno)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105824-59-7

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105824-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105824-59-7 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, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105824-59:
(8*1)+(7*0)+(6*5)+(5*8)+(4*2)+(3*4)+(2*5)+(1*9)=117
117 % 10 = 7
So 105824-59-7 is a valid CAS Registry Number.

105824-59-7SDS

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 1,2-diphenyl-2-methylseleno-propane-1-ol

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:105824-59-7 SDS

105824-59-7Downstream Products

105824-59-7Relevant articles and documents

SYNTHESIS OF α-SELENOALKYLLITHIUM COMPOUNDS

Krief, A.,Dumont, W.,Clarembeau, M.,Bernard, G.,Badaoui, E.

, p. 2005 - 2022 (2007/10/02)

α-Phenylselenoalkyllithiums and α-methylselenoalkyllithiums have been prepared from the corresponding selenoacetals and alkyllithiums.Several features of this reaction are disclosed.For example, the reaction is more readily achieved on phenylselenoacetals than on methylseleno analogues.Those derived from hindered carbonyl compounds are less readily cleaved. s-BuLi/THF proved superior to n-BuLi in THF, itself better than n-BuLi in ether.

A NOVEL METHOD FOR THE GEMINAL DIALKYLATION OF THE CARBONYL GROUP OF AROMATIC ALDEHYDES AND KETONES

Clarembeau, M.,Krief, A.

, p. 1719 - 1722 (2007/10/02)

The title transformation is efficiently achieved by using the selenium methodology which involves the sequential reductive alkylation of arylselenoacetals and of benzylselenides.

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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