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304-11-0

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304-11-0 Usage

General Description

1-(2,2-diphenylethenyl)-3-fluorobenzene is a chemical compound with the molecular formula C22H17F. It is a combination of a fluorobenzene and a diphenylethenyl group, giving it a unique structure and properties. 1-(2,2-diphenylethenyl)-3-fluorobenzene is commonly used as a building block in organic synthesis and pharmaceutical manufacturing. It is known for its fluorescent properties, making it valuable in the development of imaging agents and dyes. Additionally, 1-(2,2-diphenylethenyl)-3-fluorobenzene has potential applications in material science and as a precursor for the synthesis of various organic compounds. Its distinctive structure and versatile uses make it a valuable compound in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 304-11-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 304-11:
(5*3)+(4*0)+(3*4)+(2*1)+(1*1)=30
30 % 10 = 0
So 304-11-0 is a valid CAS Registry Number.

304-11-0SDS

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-(2,2-diphenylethenyl)-3-fluorobenzene

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:304-11-0 SDS

304-11-0Relevant articles and documents

Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source

Li, Jin,Huang, Wenhao,Chen, Jingzhi,He, Lingfeng,Cheng, Xu,Li, Guigen

supporting information, p. 5695 - 5698 (2018/04/30)

The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C?N bonds through reactions between cationic carbon species and the sulfamate.

SYNTHETIC ANTIGONADOTROPINS. 3.

FOX,GIBAS,LEE,BORIS

, p. 250 - 251 (2007/10/15)

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