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Ethanone, 2-[(3,4-dichlorophenyl)methylamino]-1-[(2S,3S)-3-phenyl-2-(1-pyrrolidinylmethyl)-1-piperidinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1034708-25-2

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1034708-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034708-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,7,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1034708-25:
(9*1)+(8*0)+(7*3)+(6*4)+(5*7)+(4*0)+(3*8)+(2*2)+(1*5)=122
122 % 10 = 2
So 1034708-25-2 is a valid CAS Registry Number.

1034708-25-2SDS

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 2-[(3,4-Dichlorophenyl)(methyl)amino]-1-[(2S,3S)-3-phenyl-2-(1-py rrolidinylmethyl)-1-piperidinyl]ethanone

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1034708-25-2 SDS

1034708-25-2Upstream product

1034708-25-2Downstream Products

1034708-25-2Relevant academic research and scientific papers

2-Aminomethyl piperidines as novel urotensin-II receptor antagonists

Jin, Jian,Wang, Yonghui,Wang, Feng,Shi, Dongchuan,Erhard, Karl F.,Wu, Zining,Guida, Brian F.,Lawrence, Sarah K.,Behm, David J.,Disa, Jyoti,Vaidya, Kalindi S.,Evans, Christopher,McMillan, Lynette J.,Rivero, Ralph A.,Neeb, Michael J.,Douglas, Stephen A.

, p. 2860 - 2864 (2008/12/22)

A series of 2-aminomethyl piperidines has been discovered as novel urotensin-II receptor antagonists. The synthesis, initial structure-activity relationships, and optimization of the initial hit that resulted in the identification of potent, cross-species active, and functional urotensin-II receptor antagonists such as 1a and 11a are described.

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