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4-fluoro-N-propan-2-yl-benzohydrazide is a chemical compound with the molecular formula C10H12FN2O. It is a derivative of benzohydrazide, featuring a fluorine atom at the 4-position and a propan-2-yl group attached to the nitrogen atom. This organic molecule is known for its potential applications in pharmaceuticals and medicinal chemistry, particularly as a building block for the synthesis of various bioactive compounds. The compound's structure allows for further functionalization and modification, making it a versatile intermediate in the development of new drugs and chemical entities.

2925-02-2

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2925-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2925-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2925-02:
(6*2)+(5*9)+(4*2)+(3*5)+(2*0)+(1*2)=82
82 % 10 = 2
So 2925-02-2 is a valid CAS Registry Number.

2925-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-N'-propan-2-ylbenzohydrazide

1.2 Other means of identification

Product number -
Other names p-Fluorobenzoic acid 2-isopropylhydrazide

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:2925-02-2 SDS

2925-02-2Relevant academic research and scientific papers

Discovery of a novel series of indolyl hydrazide derivatives as diacylglycerol acyltransferase-1 inhibitors

Kim, Minkyoung,Kwon, Jinsun,Kim, Mun Ock,Singh, Sarbjit,Kim, Sang Kyum,Lee, Kyeong,Lee, Kiho,Lee, Hyun Sun,Choi, Yongseok

supporting information, p. 628 - 635 (2015/05/04)

A novel series of hydrazide derivatives were synthesized as potential diacylglycerol acyltransferase (DGAT) inhibitors. Among them, compounds 8u and 8v exhibited selective and potent DGAT-1 inhibitory activities. In addition, compound 8u dose-dependently inhibited triglyceride synthesis in HepG2 cell lines. Furthermore, treatment with compound 8u for an oral lipid tolerance test showed a significant decrease in plasma triglyceride levels compared with vehicle-treated control animals, indicating delayed absorption of triglyceride after an acute lipid challenge.

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