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26086-06-6

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26086-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26086-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26086-06:
(7*2)+(6*6)+(5*0)+(4*8)+(3*6)+(2*0)+(1*6)=106
106 % 10 = 6
So 26086-06-6 is a valid CAS Registry Number.

26086-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl benzyl(phenyl)phosphinate

1.2 Other means of identification

Product number -
Other names Phenyl-benzyl-phosphinsaeure-methylester

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:26086-06-6 SDS

26086-06-6Relevant articles and documents

Dynamic Kinetic Resolution of Phosphinic Acid Derivatives via Nucleophilic Substitution at Phosphorus Center

Strzelecka, Dorota,Baok, Olga,Borowski, Piotr,Stankevi?, Marek

, p. 4922 - 4932 (2018/12/14)

Reaction of racemic phosphinic acid derivatives with chiral alcohols proceeds with predominant formation of one diastereomer. The highest level of enrichment has been obtained for transesterfication of racemic methyl benzylphenylphosphinate (64% de). The

Facile preparation of polymer-supported methyl sulfonate and its recyclable use for methylation of carboxylic acids and amines

Yoshino, Tomonori,Togo, Hideo

, p. 517 - 519 (2007/10/03)

A simple and efficient one-pot procedure for the preparation of polymer-supported methyl sulfonate from the reaction of polymer-supported sulfonic acid with trimethyl orthoacetate was achieved, and it could be successfully used for efficient methylation of carboxylic acids, phosphonic acids, sulfinic acids, amines, thiol, and phenol. Moreover, the polymer reagent could be recovered, regenerated, and reused easily for the same reactions. Georg Thieme Verlag Stuttgart.

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