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Benzenepropanamide, 3-nitro-β-oxo-N-phenyl-, also known as 3-nitro-N-phenyl-β-oxobenzenepropanamide, is a chemical compound with the molecular formula C15H12N2O4. It is a derivative of benzenepropanamide, featuring a nitro group (-NO2) at the 3-position, a carbonyl group (C=O) at the β-position, and a phenyl group (C6H5) attached to the nitrogen atom. Benzenepropanamide, 3-nitro-b-oxo-N-phenyl- is an organic molecule that belongs to the class of amides and is characterized by its aromatic structure and functional groups. It is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and other organic compounds. Due to its complex structure and potential reactivity, it is important to handle Benzenepropanamide, 3-nitro-b-oxo-N-phenyl- with care and in accordance with proper safety protocols.

968-00-3

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968-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 968-00-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 968-00:
(5*9)+(4*6)+(3*8)+(2*0)+(1*0)=93
93 % 10 = 3
So 968-00-3 is a valid CAS Registry Number.

968-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-nitro-phenyl)-3-oxo-propionic acid anilide

1.2 Other means of identification

Product number -
Other names 3-Nitro-benzoylessigsaeure-anilid

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:968-00-3 SDS

968-00-3Relevant academic research and scientific papers

A highly enantioselective Darzens reaction between diazoacetamides and aldehydes catalyzed by a (+)-pinanediol-Ti(OiPr)4 system

Liu, Gang,Zhang, Daming,Li, Jian,Xu, Guangyang,Sun, Jiangtao

, p. 900 - 904 (2013/02/25)

A highly efficient enantioselective Darzens reaction of aldehydes with diazoacetamides catalyzed by a (+)-pinanediol-Ti(OiPr)4 system has been developed. The cis-glycidic amides were obtained in high yields and with moderate to excellent enantioselectivity (up to 99%).

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