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4-Benzhydrylstyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47128-23-4

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47128-23-4 Usage

Uses

Monomer for the generation of stabilized radical species appended to a polymer backbone.

Check Digit Verification of cas no

The CAS Registry Mumber 47128-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,1,2 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 47128-23:
(7*4)+(6*7)+(5*1)+(4*2)+(3*8)+(2*2)+(1*3)=114
114 % 10 = 4
So 47128-23-4 is a valid CAS Registry Number.

47128-23-4 Well-known Company Product Price

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  • Aldrich

  • (725595)  4-Benzhydrylstyrene  96%

  • 47128-23-4

  • 725595-1G

  • 1,736.28CNY

  • Detail

47128-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzhydryl-4-ethenylbenzene

1.2 Other means of identification

Product number -
Other names 4-Benzhydrylstyrene

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:47128-23-4 SDS

47128-23-4Upstream product

47128-23-4Relevant academic research and scientific papers

Synthesis of Triarylmethanes via Palladium-Catalyzed Suzuki Coupling of Trimethylammonium Salts and Arylboronic Acids

Zhang, Zhenming,Wang, Hui,Qiu, Nianli,Kong, Yujing,Zeng, Wenjuan,Zhang, Yongquan,Zhao, Junfeng

, p. 8710 - 8715 (2018)

An efficient palladium-catalyzed Suzuki coupling of 1,1-diarylmethyl-trimethylammonium triflates with arylboronic acids is reported. This reaction offers a novel approach to triarylmethane derivatives in good to excellent yields with the palladium-catalyzed C-N bond cleavage as the key feature. Broad substrate scope regarding both reaction partners are observed. Moreover, reactive functional groups such as vinyl and formyl groups are conserved in this transformation.

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