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Benzamide,5-bromo-N-[[(2S)-1-[(4-fluorophenyl)methyl]-2-pyrrolidinyl]methyl]-2,3-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107188-86-3

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107188-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107188-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,8 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107188-86:
(8*1)+(7*0)+(6*7)+(5*1)+(4*8)+(3*8)+(2*8)+(1*6)=133
133 % 10 = 3
So 107188-86-3 is a valid CAS Registry Number.

107188-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-N-[(S)-1-(4-fluoro-benzyl)-pyrrolidin-2-ylmethyl]-2,3-dimethoxy-benzamide

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:107188-86-3 SDS

107188-86-3Downstream Products

107188-86-3Relevant academic research and scientific papers

Potential antipsychotic agents. 9. Synthesis and stereoselective dopamine D-2 receptor blockade of a potent class of substituted (R)-N-[(1-benzyl-2-pyrrolidinyl)methyl]benzamides. Relations to other side chain congeners

Hogberg,Strom,De Paulis,Stensland,Csoregh,Lundin,Hall,Ogren

, p. 948 - 955 (2007/10/02)

A number of substituted N-[(1-benzyl-2-pyrrolidinyl)methyl]benzamides and -salicylamides have been prepared and investigated as dopamine D-2 receptor antagonists in vitro and in vivo. The affinity was found to be confined to the R enantiomer, in contrast

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