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17038-84-5

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17038-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17038-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,3 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17038-84:
(7*1)+(6*7)+(5*0)+(4*3)+(3*8)+(2*8)+(1*4)=105
105 % 10 = 5
So 17038-84-5 is a valid CAS Registry Number.

17038-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-benzoyl-3-methyl-4-oxo-3-piperidinecarboxylate

1.2 Other means of identification

Product number -
Other names 1-benzoyl-3-methyl-4-oxo-piperidine-3-carboxylic acid ethyl ester

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:17038-84-5 SDS

17038-84-5Relevant articles and documents

The search for TCP analogues binding to the low affinity PCP receptor sites in the rat cerebellum

Hamon, Jacques,Espaze, Florence,Vignon, Jacques,Kamenka, Jean-Marc

, p. 125 - 135 (2007/10/03)

With the aim of obtaining selective ligands of the low affinity binding sites of [3H]-1-[1-(2-thienyl)cyclohexyl]piperidine ([3H]TCP) in the rat cerebellum, oxygen and sulfur atoms were introduced in the TCP structure and derivatives to obtain analogues with a lowered lipophilicity. These compounds, and others already obtained, were assayed comparatively to determine their affinities for three sites labeled with [3H]TCP: one in the forebrain, the originally described PCP receptor, and two in the rat cerebellum. Lowering the lipophilicity and modifying the hetero-aromatic moiety yielded some ligands with increased affinity for the low affinity sites in the rat cerebellum and decreased affinity for the high affinity sites in the forebrain. Particularly, two compounds displaying both a high affinity and a good selectivity might be valuable tools to elucidate the pharmacology of the low affinity PCP sites labeled with [3H]TCP in the rat cerebellum.

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