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Ethanone, 2-diazo-1-(3-fluorophenyl)-, also known as 2-diazo-1-(3-fluorophenyl)ethanone, is an organic compound characterized by its unique chemical structure. It features a diazoketone functional group, which consists of a carbonyl group (C=O) bonded to a diazo group (N2) and a fluorophenyl group. The fluorophenyl group has a fluorine atom attached to the third carbon of the benzene ring, which imparts specific electronic and steric properties to the molecule. Ethanone, 2-diazo-1-(3-fluorophenyl)- is of interest in organic chemistry and synthetic chemistry due to its potential applications in the formation of various complex molecules and its reactivity in chemical transformations. It is important to handle such compounds with care, as diazo compounds can be reactive and potentially hazardous.

6929-49-3

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6929-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6929-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6929-49:
(6*6)+(5*9)+(4*2)+(3*9)+(2*4)+(1*9)=133
133 % 10 = 3
So 6929-49-3 is a valid CAS Registry Number.

6929-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Fluor-ω-diazo-acetophenon

1.2 Other means of identification

Product number -
Other names m-Fluor-diazoacetophenon

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:6929-49-3 SDS

6929-49-3Relevant academic research and scientific papers

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

Young, Jonathan R.,Huang, Song X.,Chen, Irene,Walsh, Thomas F.,DeVita, Robert J.,Wyvratt Jr., Matthew J.,Goulet, Mark T.,Ren, Ning,Lo, Jane,Yang, Yi Tien,Yudkovitz, Joel B.,Cheng, Kang,Smith, Roy G.

, p. 1723 - 1727 (2007/10/03)

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.

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