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7023-79-2

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7023-79-2 Usage

General Description

Ethanone, 1-(3-bromophenyl)-2-diazo- is a chemical compound that belongs to the group of diazo compounds, which are known for their reactivity and use in various chemical reactions. This specific compound contains a ketone group attached to a phenyl ring with a bromine substituent at the 3-position. The diazo group, characterized by the presence of two nitrogen atoms double-bonded to each other, adds further to the reactivity of this compound. Due to its diazo group, Ethanone, 1-(3-bromophenyl)-2-diazo- is often utilized in organic synthesis as a diazo transfer reagent, enabling the introduction of the diazo group into other molecules for the purpose of functionalization and modification. It is important to handle this compound with caution, as diazo compounds are known for their explosive properties and must be handled carefully in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 7023-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7023-79:
(6*7)+(5*0)+(4*2)+(3*3)+(2*7)+(1*9)=82
82 % 10 = 2
So 7023-79-2 is a valid CAS Registry Number.

7023-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)-2-diazonioethenolate

1.2 Other means of identification

Product number -
Other names m-bromobenzoyl diazomethane

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:7023-79-2 SDS

7023-79-2Relevant articles and documents

Synthesis of the Potent, Selective, and Efficacious β-Secretase (BACE1) Inhibitor NB-360

Rueeger, Heinrich,Lueoend, Rainer,Machauer, Rainer,Veenstra, Siem J.,Holzer, Philipp,Hurth, Konstanze,Voegtle, Markus,Frederiksen, Mathias,Rondeau, Jean-Michel,Tintelnot-Blomley, Marina,Jacobson, Laura H.,Staufenbiel, Matthias,Laue, Grit,Neumann, Ulf

supporting information, p. 4677 - 4696 (2021/05/06)

Starting from lead compound 4, the 1,4-oxazine headgroup was optimized to improve potency and brain penetration. Focusing at the 6-position of the 5-amino-1,4-oxazine, the insertion of a Me and a CF3 group delivered an excellent pharmacological profile wi

One-pot synthesis of polyfunctional pyrazoles: An easy access to α-diazoketones from arylglyoxal monohydrates and tosylhydrazine

Shu, Wen-Ming,Ma, Jun-Rui,Zheng, Kai-Lu,Sun, Hui-Ying,Wang, Mei,Yang, Yan,Wu, An-Xin

, p. 9321 - 9329 (2015/03/05)

A new and efficient method for the generation of α-diazoketones has been developed from arylglyoxal monohydrates and tosylhydrazine at room temperature. 1,3-Dipolar cycloaddition reactions were used to constructing polyfunctional pyrazole derivatives by the reaction of generated α-diazoketones in situ with electron-deficient alkenes, quinones and coumarins in one pot. The one-dimensional molecular packing of 1H-benzo[f]indazole-4,9-dione derivatives along the c direction demonstrated a helical chain formation via N-H?O hydrogen-bonding.

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