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9-Azabicyclo[6.1.0]non-9-yl(4-nitrophenyl)methanone is a complex organic compound with the molecular formula C15H18N2O3. It features a 9-azabicyclo[6.1.0]nonane ring, which is a nine-membered ring with one nitrogen atom, and a 4-nitrophenyl group attached to a central carbonyl group. 9-azabicyclo[6.1.0]non-9-yl(4-nitrophenyl)methanone is characterized by its unique molecular structure, which includes a cyclic amine and a nitrophenyl moiety. It is a white crystalline solid and is typically used in the synthesis of various pharmaceuticals and chemical intermediates due to its reactive functional groups. The compound's properties, such as its solubility and reactivity, can be influenced by the presence of the nitro group, which can participate in various chemical reactions, making it a potentially valuable building block in organic synthesis.

21392-68-7

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21392-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21392-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21392-68:
(7*2)+(6*1)+(5*3)+(4*9)+(3*2)+(2*6)+(1*8)=97
97 % 10 = 7
So 21392-68-7 is a valid CAS Registry Number.

21392-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-azabicyclo[6.1.0]nonan-9-yl-(4-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names 9-(4-Nitro-benzoyl)-9-aza-bicyclo<6.1.0>nonan

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

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More Details:21392-68-7 SDS

21392-68-7Relevant academic research and scientific papers

RuV-Acylimido Intermediate in [RuIV(Por)Cl2]-Catalyzed C–N Bond Formation: Spectroscopic Characterization, Reactivity, and Catalytic Reactions

Che, Chi-Ming,Hong, Dan-Yan,Huang, Jie-Sheng,Law, Siu-Man,Liu, Yungen,Lo, Vanessa Kar-Yan,Toy, Patrick H.,Wu, Liangliang

supporting information, p. 18619 - 18629 (2021/06/09)

Metal-catalyzed C?N bond formation reactions via acylnitrene transfer have recently attracted much attention, but direct detection of the proposed acylnitrenoid/acylimido M(NCOR) (R=aryl or alkyl) species in these reactions poses a formidable challenge. H

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