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210346-38-6

4-(4-fluoro-5-Methyl-2-nitrophenyl)butanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210346-38-6

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210346-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210346-38-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,4 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 210346-38:
(8*2)+(7*1)+(6*0)+(5*3)+(4*4)+(3*6)+(2*3)+(1*8)=86
86 % 10 = 6
So 210346-38-6 is a valid CAS Registry Number.

210346-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-Fluoro-5-methyl-2-nitrophenyl)butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(4-fluoro-5-methyl-2-nitrophenyl)butyric acid

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:210346-38-6 SDS

210346-38-6Relevant articles and documents

Preparation method of o-acetamidobenzenebutyric acid compound

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Paragraph 0043-0047, (2021/02/10)

The invention discloses a preparation method of an o-acetamidobenzenebutyric acid compound. The o-acetamidobenzenebutyric acid compound is prepared through a reaction route as shown in a formula A, wherein R1 represents a C1-6 alkyl group, R2 represents a

Synthesis and antitumor activity of ring A- and F-modified hexacyclic camptothecin analogues

Sugimori, Masamichi,Ejima, Akio,Ohsuki, Satoru,Uoto, Kouichi,Mitsui, Ikuo,Kawato, Yasuyoshi,Hirota, Yasuhide,Sato, Keiki,Terasawa, Hirofumi

, p. 2308 - 2318 (2007/10/03)

Nineteen ring A- and F-modified hexacyclic analogues of camptothecin were synthesized by Friedlander condensation of appropriately substituted bicyclic amino ketones with tricyclic ketone and were evaluated for cytotoxicity and topoisomerase I inhibitory

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