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501085-54-7

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501085-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501085-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,8 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 501085-54:
(8*5)+(7*0)+(6*1)+(5*0)+(4*8)+(3*5)+(2*5)+(1*4)=107
107 % 10 = 7
So 501085-54-7 is a valid CAS Registry Number.

501085-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2-(dimethoxymethyl)phenol

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-dimethoxymethyl-phenol

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:501085-54-7 SDS

501085-54-7Relevant articles and documents

Method for preparing vilazodone intermediate through copper-catalyzed coupling reaction

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Paragraph 0037; 0047-0049; 0056-0058; 0066-0068, (2021/08/07)

The invention discloses a method for preparing a vilazodone intermediate through a copper-catalyzed coupling reaction. The method comprises the following steps: step 1, generating 2-hydroxy-5-bromobenzene dimethyl acetal (IV) from 2-hydroxy-5-bromobenzald

Long-range diastereoselectivity in an Ugi reaction: Stereocontrolled and diversity-oriented synthesis of tetrahydrobenzoxazepines

Banfi, Luca,Bagno, Alessandro,Basso, Andrea,De Santis, Carlo,Riva, Renata,Rastrelli, Federico

, p. 5064 - 5075 (2013/11/06)

Salicylaldehydes and protected 1,2-amino alcohols have been convergently converted into a series of 2,3-dihydrobenzo[f][1,4]oxazepines, which undergo an Ugi-Joullie multicomponent reaction with unusual long-range diastereoselectivity. This protocol allows

RHODANDSE DERIVARIVES, A PROCESS FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING THE SAME

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Page/Page column 20, (2010/11/28)

Disclosed herein are rhodanine derivatives, a method for the preparation thereof, and a pharmaceutical composition containing the same. The rhodanine derivatives have inhibitory activity against protein phosphatases (PPase) such as PTPlB, Prl-3, LAR, CD45

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