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831-93-6

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831-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 831-93-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 831-93:
(5*8)+(4*3)+(3*1)+(2*9)+(1*3)=76
76 % 10 = 6
So 831-93-6 is a valid CAS Registry Number.

831-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylmethoxypentan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Benzyloxy-pentan-2-ol

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:831-93-6 SDS

831-93-6Relevant articles and documents

PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 142, (2020/01/11)

Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS.

Convenient synthesis of monoprotected 1,2-diols

Poppe,Recseg,Novak

, p. 3993 - 4000 (2007/10/03)

Reaction of the protected glycidol derivatives (1A-C) with a wide variety of Grignard reagents (2a-h) in the presence of catalytic amount of CuCN provided the corresponding monoprotected diol derivatives (3) in a highly regioselective manner.

A NEW METHOD FOR THE HYDROXYMETHYLATION OF CARBONYL COMPOUNDS

Imamoto, Tsuneo,Takeyama, Toshiaki,Yokoyama, Masataka

, p. 3225 - 3226 (2007/10/02)

Benzyl chloromethyl ether reacts with carbonyl compounds in the presence of SmI2 to afford alcohols (I), which are subsequently subjected to hydrogenolysis to yield diols (II).

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