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1085313-37-6

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1085313-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1085313-37-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,5,3,1 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1085313-37:
(9*1)+(8*0)+(7*8)+(6*5)+(5*3)+(4*1)+(3*3)+(2*3)+(1*7)=136
136 % 10 = 6
So 1085313-37-6 is a valid CAS Registry Number.

1085313-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-(4-methylbenzylideneamino)ethyl)phenol

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:1085313-37-6 SDS

1085313-37-6Relevant articles and documents

Syntheses of a selective peroxisome proliferator activated receptor modulator and practical new preparations of 2-(4-Alkoxyphenyl) ethylamines t

Magnus, Nicholas A.,Astleford, Bret A.,Brennan, John,Stout, James R.,Tharp-Taylor, Roger W.

experimental part, p. 280 - 284 (2010/04/22)

This article describes chemistry that was developed to give access to multigram quantities of the selective peroxisome proliferator activated receptor modulator (SPPARM), compound 1.1 Fischer esteriflcations, phase transfer-catalyzed alkylations, amide couplings, crystallizations, and a new synthesis were developed to accomplish this task. In addition, an efficient method for preparing 2-(4-alkoxyphenyl) ethylamines 7a - d from tyramine 9 was developed that involves O-alkylation of intermediate Schiff base 11 and subsequent acid-catalyzed hydrolysis to afford the target molecules as crystalline hydrochloride salts.

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