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1-(4-Chlorobenzoyl)-3-Methylpiperidine, 97% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19202-07-4

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19202-07-4 Usage

Composition

Piperidine ring with a 4-chlorobenzoyl group attached to the 1 position and a methyl group attached to the 3 position

Physical State

White crystalline solid

Purity

97%

Usage

Pharmaceutical industry as an intermediate in the synthesis of various drugs and compounds

Check Digit Verification of cas no

The CAS Registry Mumber 19202-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19202-07:
(7*1)+(6*9)+(5*2)+(4*0)+(3*2)+(2*0)+(1*7)=84
84 % 10 = 4
So 19202-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16ClNO/c1-10-3-2-8-15(9-10)13(16)11-4-6-12(14)7-5-11/h4-7,10H,2-3,8-9H2,1H3

19202-07-4SDS

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 (4-chlorophenyl)-(3-methylpiperidin-1-yl)methanone

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:19202-07-4 SDS

19202-07-4Downstream Products

19202-07-4Relevant academic research and scientific papers

Piperidyl amides as novel, potent and orally active mGlu5 receptor antagonists with anxiolytic-like activity

Spanka, Carsten,Glatthar, Ralf,Desrayaud, Sandrine,Fendt, Markus,Orain, David,Troxler, Thomas,Vranesic, Ivo

scheme or table, p. 184 - 188 (2010/04/24)

High throughput screening led to the identification of nicotinamide derivative 2 as a structurally novel mGluR5 antagonist. Optimization of the modular scaffold led to the discovery of 16m, a compound with high affinity for mGluR5 and excellent selectivit

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