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1-oxo-3-phenyl-1-pyrrolidin-1-ylpropan-2-amine is a complex organic compound with the molecular formula C12H16N2O. It is a derivative of proline, an amino acid, and features a pyrrolidine ring, a phenyl group, and an amide group. 1-oxo-3-phenyl-1-pyrrolidin-1-ylpropan-2-amine is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is often used as an intermediate in the preparation of various drugs and bioactive molecules, showcasing its importance in the field of medicinal chemistry.

92032-60-5

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92032-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92032-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,3 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92032-60:
(7*9)+(6*2)+(5*0)+(4*3)+(3*2)+(2*6)+(1*0)=105
105 % 10 = 5
So 92032-60-5 is a valid CAS Registry Number.

92032-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-phenyl-1-(1-pyrrolidinyl)-1-propanone

1.2 Other means of identification

Product number -
Other names Aziridin-carbonsaeure-(1)-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:92032-60-5 SDS

92032-60-5Relevant academic research and scientific papers

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

Zhu, Mingzhao,Zheng, Nan

, p. 2223 - 2236 (2011/09/15)

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.

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