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102762-46-9

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102762-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102762-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,6 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102762-46:
(8*1)+(7*0)+(6*2)+(5*7)+(4*6)+(3*2)+(2*4)+(1*6)=99
99 % 10 = 9
So 102762-46-9 is a valid CAS Registry Number.

102762-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-phenyl-1-(3-phenylpropyl)piperidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Phenyl-1-(3-phenyl-propyl)-piperidin-4-carbonsaeure-aethylester

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:102762-46-9 SDS

102762-46-9Downstream Products

102762-46-9Relevant articles and documents

Structure-activity relationship exploration of Kv1.3 blockers based on diphenoxylate

Nguyen, William,Howard, Brittany L.,Jenkins, David P.,Wulff, Heike,Thompson, Philip E.,Manallack, David T.

supporting information, p. 7106 - 7109 (2013/01/15)

Diphenoxylate, a well-known opioid agonist and anti-diarrhoeal agent, was recently found to block Kv1.3 potassium channels, which have been proposed as potential therapeutic targets for a range of autoimmune diseases. The molecular basis for this Kv1.3 blockade was assessed by the selective removal of functional groups from the structure of diphenoxylate as well as a number of other structural variations. Removal of the nitrile functional group and replacement of the C-4 piperidinyl substituents resulted in several compounds with submicromolar IC50 values.

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