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3-benzo[1,3]dioxol-5-yl-4-nitro-1-phenyl-butan-1-one is a complex organic compound characterized by a molecular structure that includes a benzodioxole ring, a nitro group, and a phenyl group. The benzodioxole ring, which is a six-membered aromatic ring with two oxygen atoms, is attached to a butanone chain. The butanone chain has four carbon atoms, with the first carbon being part of the benzodioxole ring, the second carbon bearing a nitro group, and the third carbon connected to a phenyl group. The fourth carbon is the ketone carbonyl group. 3-benzo[1,3]dioxol-5-yl-4-nitro-1-phenyl-butan-1-one is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates, particularly those involving the benzodioxole moiety, which can contribute to the compound's biological activity.

6947-83-7

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6947-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6947-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6947-83:
(6*6)+(5*9)+(4*4)+(3*7)+(2*8)+(1*3)=137
137 % 10 = 7
So 6947-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO5/c19-15(12-4-2-1-3-5-12)8-14(10-18(20)21)13-6-7-16-17(9-13)23-11-22-16/h1-7,9,14H,8,10-11H2

6947-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,3-benzodioxol-5-yl)-4-nitro-1-phenylbutan-1-one

1.2 Other means of identification

Product number -
Other names -

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:6947-83-7 SDS

6947-83-7Relevant academic research and scientific papers

Sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes: one-step synthesis of 4-nitro-1,3-diarylbutan-1-ones

Li, Zheng,Lu, Hao,Liu, Zhenrong,Ma, Xiaolong

, (2019/03/29)

Abstract : The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild, transition-metal-free condition. This one-step method involving sequential carbon-carbon bond formation and cleavage provides a good alternative to the synthesis of various γ-nitro ketones. Graphical abstract: The sequential Michael addition/retro-Claisen condensation of 1,3-diarylpropan-1,3-diones with nitrostyrenes is described. 4-Nitro-1,3-diarylbutan-1-ones were efficiently synthesized in good to high yield under mild and transition-metal-free condition. [Figure not available: see fulltext.].

Enantioselective addition of aryl ketones and acetone to nitroalkenes organocatalyzed by carbamate-monoprotected cyclohexa-1,2-diamines

Flores-Ferrndiz, Jess,Stiven, Alexander,Sotorros, Lia,Gmez-Bengoa, Enrique,Chinchilla, Rafael

, p. 970 - 979 (2015/09/01)

Enantiomerically pure carbamate-monoprotected trans-cyclohexane-1,2-diamines are used as chiral organocatalysts for the addition of aryl ketones and acetone to nitroalkenes to give enantioenriched β-substituted γ-nitroketones. The reaction was performed i

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