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58005-47-3

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58005-47-3 Usage

Structure

Biphenyl derivative with two methoxy groups and one methyl group attached to the benzene rings

Usage

a. Organic synthesis
b. Pharmaceutical research
c. Building block for various pharmaceuticals and organic compounds
d. Standard reference material in analytical chemistry

Biological and pharmacological properties

Studied for potential properties

Safety

Handle with care, follow proper safety protocols and guidelines due to potential hazards and health risks

Check Digit Verification of cas no

The CAS Registry Mumber 58005-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,0 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58005-47:
(7*5)+(6*8)+(5*0)+(4*0)+(3*5)+(2*4)+(1*7)=113
113 % 10 = 3
So 58005-47-3 is a valid CAS Registry Number.

58005-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethoxy-5-methyl-2-phenylcyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,1-biphenyl,2,4-dimethoxy-4-methyl

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:58005-47-3 SDS

58005-47-3Downstream Products

58005-47-3Relevant articles and documents

A Molecular/Heterogeneous Nickel Catalyst for Suzuki-Miyaura Coupling

Key, Ryan J.,Tengco, John Meynard M.,Smith, Mark D.,Vannucci, Aaron K.

, p. 2007 - 2014 (2019/05/16)

A molecular/heterogeneous catalyst motif based on an earth abundant nickel catalyst and SiO2 support has been designed and synthesized. Characterization and catalytic testing indicate that the molecular nickel catalyst [(2,2′:6′,2′′-terpyridine-4′-benzoic acid)Ni(II)]Cl2 attached to a high surface area SiO2 support is the active cross-coupling catalyst and increased product yields are a result of increased molecular stability of the catalyst while attached to the SiO2 support. This molecular/heterogeneous motif is easily separated from reaction mixtures and can be recycled for multiple catalytic reactions. The catalyst is active for Suzuki-Miyaura catalysis at catalyst loadings as low as 0.1 mol %, and turnover numbers nearing 2000 have been achieved.

Palladium-catalyzed coupling of organolead compounds with organoboranes

Kang, Suk-Ku,Ryu, Hyung-Chul,Son, Hoe-Joo

, p. 771 - 773 (2007/10/03)

The palladium-catalyzed cross-coupling of organolead compounds with organoboranes was carried out in the presence of Pd2(dba)3-CHCl3 (5 mol %), CuI (10 mol %), and NaOMe (6 equiv) in CH3CNXDME (1 : 1) under mild conditions.

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