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181641-74-7

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181641-74-7 Usage

Chemical class

Piperidinecarboxylic acids

Composition

Piperidine ring with two phenylmethyl groups attached at the 1 and 4 positions

Industry use

Pharmaceutical industry as a building block for drug synthesis

Known properties

Potential antihypertensive and antiarrhythmic properties

Research focus

Treatment of neurological disorders and neurodegenerative diseases

Pharmacological potential

Significant due to its various therapeutic applications

Ongoing research

Further exploration of its therapeutic applications and properties

Check Digit Verification of cas no

The CAS Registry Mumber 181641-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,6,4 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 181641-74:
(8*1)+(7*8)+(6*1)+(5*6)+(4*4)+(3*1)+(2*7)+(1*4)=137
137 % 10 = 7
So 181641-74-7 is a valid CAS Registry Number.

181641-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Dibenzyl-4-carboxypiperidine

1.2 Other means of identification

Product number -
Other names 1,4-Bis-benzyl-4-piperidinecarboxylicacid

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:181641-74-7 SDS

181641-74-7Upstream product

181641-74-7Downstream Products

181641-74-7Relevant articles and documents

The design and discovery of novel amide CCR5 antagonists

Pryde, David C.,Corless, Martin,Fenwick, David R.,Mason, Helen J.,Stammen, Blanda C.,Stephenson, Peter T.,Ellis, David,Bachelor, David,Gordon, David,Barber, Christopher G.,Wood, Anthony,Middleton, Donald S.,Blakemore, David C.,Parsons, Gemma C.,Eastwood, Rachel,Platts, Michelle Y.,Statham, Keith,Paradowski, Kerry A.,Burt, Catherine,Klute, Wolfgang

supporting information; scheme or table, p. 1084 - 1088 (2009/08/07)

The synthesis of a range of novel amine-containing structures and their primary potency as inhibitors of HIV-1 fusion via blocking of the CCR5 receptor is described. The development of the medicinal chemistry strategy and SAR's which led to the identification of the piperidine amide compounds 33 and 36 as excellent leads for further evaluation is described, along with key physicochemical data which highlighted their lead potential.

PIPERIDINE DERIVATIVES, PROCESS FOR OBTAINING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

-

, (2008/06/13)

Piperidine derivatives, process for obtaining them and pharmaceutical compositions containing them, of formula STR1 used as neurokinin receptor antagonists, which are, in particular, useful for the treatment of all substance P-and neurokinin-dependent pathologies.

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