Cas 86956-38-9,1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide

86956-38-9

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Basic information

Product Name: 1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide
Synonyms: 1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide
CAS NO:86956-38-9
Molecular Formula:
Molecular Weight: 325.838
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide(86956-38-9)
EPA Substance Registry System: 1-Propyl-piperidine-4-carboxylic acid (4-amino-5-chloro-2-methoxy-phenyl)-amide(86956-38-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 86956-38-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86956-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,5 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86956-38:
(7*8)+(6*6)+(5*9)+(4*5)+(3*6)+(2*3)+(1*8)=189
189 % 10 = 9
So 86956-38-9 is a valid CAS Registry Number.

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86956-38-9Relevant academic research and scientific papers

Anilides Related to Substituted Benzamides. Potential Antipsychotic Activity of N-(4-Amino-5-chloro-2-methoxyphenyl)-1-(phenylmetyl)-4-piperidinecarboxamide

Blaney, Frank E.,Clark, Michael S. G.,Gardner, Derek V.,Hadley, Michael S.,Middleton, David,White , Trevor J.

, p. 1747 - 1752 (2007/10/02)

The substituted benzamides are used clinically both as antipsychotics and as stimulants of gastric motility.The antipsychotic effects are considered to be a consequence of their central dopamine antagonist properties, but there is evidence that the gastri

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