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(3-bromo-4-isopropoxyphenyl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

454186-08-4

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454186-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 454186-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,4,1,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 454186-08:
(8*4)+(7*5)+(6*4)+(5*1)+(4*8)+(3*6)+(2*0)+(1*8)=154
154 % 10 = 4
So 454186-08-4 is a valid CAS Registry Number.

454186-08-4SDS

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 (3-Bromo-4-isopropoxyphenyl)methanol

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:454186-08-4 SDS

454186-08-4Downstream Products

454186-08-4Relevant academic research and scientific papers

INHIBITORS OF ACETYL-COA CARBOXYLASE

-

Page/Page column 37, (2010/11/17)

The present invention relates to compounds that act as acetyl-CoA carboxylase (ACC) inhibitors. The invention also relates to methods of preparing the compounds, compositions containing the compounds, and to methods of treatment using the compounds.

First enantioselective total synthesis of (-)-tejedine

Wang, You-Chu,Georghiou, Paris E.

, p. 2675 - 2678 (2007/10/03)

(Matrix presented) The first enantioselective total synthesis of (-)-tejedine (1) is reported. Tejedine is a seco-bisbenzyltetrahydroisoquinoline isolated in 1998 as a minor component from Berberis vulgaris. The synthesis was achieved using a strategy employing four key steps, including a chiral auxiliary-assisted diastereoselective Bischler-Napieralski cyclization.

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