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5002-30-2

5002-30-2

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5002-30-2 Usage

General Description

Ethyl 2'-fluoro-4-biphenylylacetate is a chemical compound with the molecular formula C16H13FO2. It is a derivative of biphenyl and contains a fluorine atom and an ethyl ester group. ETHYL 2'-FLUORO-4-BIPHENYLYLACETATE may have applications in the fields of organic synthesis, pharmaceuticals, and materials science. It is important to handle and use this chemical with proper care, following all safety guidelines and regulations to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 5002-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5002-30:
(6*5)+(5*0)+(4*0)+(3*2)+(2*3)+(1*0)=42
42 % 10 = 2
So 5002-30-2 is a valid CAS Registry Number.

5002-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(2'-fluoro-[1,1'-biphenyl]-4-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-[4-(2-fluorophenyl)phenyl]acetate

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:5002-30-2 SDS

5002-30-2Upstream product

5002-30-2Downstream Products

5002-30-2Relevant articles and documents

Therapeutically active phenylalkane derivatives

-

, (2008/06/13)

2-(2-Fluoro-4-biphenylyl)propan-1-ol, 2-(2'-Fluoro-4-biphenylyl)propan-1-ol and 2-(2,2'-Difluoro-4-biphenylyl)propan-1-ol Possessing great anti-inflammatory, analgesic and antipyretic activities.

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