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Acetic acid, 2-oxo-2-[[(1R)-1-phenylethyl]amino]-, hydrazide is a complex organic compound with the chemical formula C10H12N2O2. It is a derivative of acetic acid, featuring a hydrazide group and a chiral phenylethylamine moiety. Acetic acid,2-oxo-2-[[(1R)-1-phenylethyl]amino]-, hydrazide is characterized by its asymmetric carbon atom, indicated by the (1R) configuration, which influences its stereochemistry. It is a white crystalline solid and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its reactivity, it is typically handled with care in a laboratory setting.

6152-23-4

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6152-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6152-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6152-23:
(6*6)+(5*1)+(4*5)+(3*2)+(2*2)+(1*3)=74
74 % 10 = 4
So 6152-23-4 is a valid CAS Registry Number.

6152-23-4SDS

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 2-hydrazinyl-2-oxo-N-(1-phenylethyl)acetamide

1.2 Other means of identification

Product number -
Other names METHYL (S)-2-FLUOROPROPIONATE

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:6152-23-4 SDS

6152-23-4Relevant academic research and scientific papers

Stereospecificity of myofibrillar calcium sensitivity and PDE inhibition in cardiotonic thiadiazinones

Nadler,Delimoge,Lahouratate,Leger,Morvan,Zimmermann

, p. 805 - 812 (2007/10/03)

In pyridazinone or thiadiazinone cardiotonic agents with one chiral centre, the PDE inhibitory action resides mainly in one enantiomer and the myofibrillar calcium sensitization mainly in the other. This phenomenon is observed when the chiral centre is located on the pyridazinone or thiadiazinone heterocycle but cannot be extended to structures where the chiral centre is elsewhere on the molecule. For the first time a stereoselective synthesis of a 5-substituted 3,6-dihydro-6-methyl-2H-1,3,4-thiadiazine-2-one has been achieved and an absolute configuration is proposed.

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