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6195-80-8

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6195-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6195-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6195-80:
(6*6)+(5*1)+(4*9)+(3*5)+(2*8)+(1*0)=108
108 % 10 = 8
So 6195-80-8 is a valid CAS Registry Number.

6195-80-8SDS

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 2-[3-(1,3-benzodioxol-5-yl)-4-oxoquinazolin-2-yl]sulfanyl-N-ethyl-N-(3-methylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2,4-Dibenzyloxyphenol

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:6195-80-8 SDS

6195-80-8Relevant articles and documents

Stereoselective deoxygenation of myo-inositol monotosylates with lithium triethylborohydride

Yu, Jinquan,Spencer, Jonathan B.

, p. 3234 - 3235 (1996)

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Tyrosinase inhibitor

-

, (2019/04/02)

PROBLEM TO BE SOLVED: To provide a new resorcinol derivative, and further, to provide a new tyrosinase activity inhibitor composed of the resorcinol derivative. SOLUTION: There are provided the resorcinol derivative, represented by formula 1, and th

A formal synthesis of valiolamine from myo-inositol

Jagdhane, Rajendra C.,Shashidhar, Mysore S.

, p. 7963 - 7970 (2011/11/14)

An efficient formal synthesis of racemic valiolamine starting from readily available myo-inositol is reported. In all the synthetic steps only one regioisomer is formed, which circumvents laborious purification of products. Regioselective benzylation of myo-inositol orthoformate, super-hydride mediated deoxygenation of a cyclitol derivative and stereoselective addition of dichloromethyllithium to an inosose are the key reactions in the synthesis.

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