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[1,1'-biphenyl]-4-yl 4-methoxybenzoate is a complex organic chemical compound with the molecular formula C19H16O3. It is a derivative of biphenyl, which is a type of aromatic hydrocarbon consisting of two phenyl rings connected by a single bond. In [1,1'-biphenyl]-4-yl 4-methoxybenzoate, one of the phenyl rings is substituted with a 4-methoxybenzoate group, which is a benzoate ester with a methoxy group attached to the para position. This molecule is characterized by its unique structure and properties, making it potentially useful in various chemical and pharmaceutical applications. However, further research and analysis are required to fully understand its potential uses and effects.

55673-00-2

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55673-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55673-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55673-00:
(7*5)+(6*5)+(5*6)+(4*7)+(3*3)+(2*0)+(1*0)=132
132 % 10 = 2
So 55673-00-2 is a valid CAS Registry Number.

55673-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-phenylphenyl) 4-methoxybenzoate

1.2 Other means of identification

Product number -
Other names 4-Biphenylyl-4''-methoxybenzoat

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:55673-00-2 SDS

55673-00-2Downstream Products

55673-00-2Relevant academic research and scientific papers

Transition-Metal-Free DMAP-Mediated Aromatic Esterification of Amides with Organoboronic Acids

Guo, Jiarui,Liu, Lantao,Wang, Tao,Wang, Yanqing,Xu, Kai,Zhang, Yuheng

supporting information, p. 3274 - 3277 (2021/06/26)

A new, transition-metal-free, effective method for aromatic esterification of amides with organoboronic acids has been developed. A wide range of benzoate derivatives were obtained with yields ranging from moderate to good. The catalytic reaction shows a broad substrate scope and excellent functional group tolerance. Conceptually, DMAP mediates the reaction and is crucial for this transformation.

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