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62790-77-6

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62790-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62790-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62790-77:
(7*6)+(6*2)+(5*7)+(4*9)+(3*0)+(2*7)+(1*7)=146
146 % 10 = 6
So 62790-77-6 is a valid CAS Registry Number.

62790-77-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name t-butyldimethylsilyloxy-3-methoxybenzene

1.2 Other means of identification

Product number -
Other names 3-(tert-Butyl-dimethylsilyloxy)anisole

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:62790-77-6 SDS

62790-77-6Relevant articles and documents

Synthesis method of 2-bromo-5-methoxyphenol

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Paragraph 0046-0049; 0057-0059, (2019/10/22)

The invention discloses a synthesis method of 2-bromo-5-methoxyphenol. According to the synthesis method, 3-methoxyphenol is taken as a raw material, firstly, the 3-methoxyphenol reacts with a protection reagent such as tert-butyldimethylsilyl chloride, a

Catalyst for aromatic C—O, C—N, and C—C bond formation

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, (2008/06/13)

The present invention is directed to a transition metal catalyst, comprising a Group 8 metal and a ligand having the structure wherein R, R′ and R″ are organic groups having 1-15 carbon atoms, n=1-5, and m=0-4. The present invention is also directed to a method of forming a compound having an aromatic or vinylic carbon-oxygen, carbon-nitrogen, or carbon-carbon bond using the above catalyst. The catalyst and the method of using the catalyst are advantageous in preparation of compounds under mild conditions of approximately room temperature and pressure.

Unusual in situ ligand modification to generate a catalyst for room temperature aromatic C-O bond formation [8]

Shelby,Kataoka,Mann,Hartwig

, p. 10718 - 10719 (2007/10/03)

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