Cas 209349-47-3,N-Methyl-N-(3-phenyl-5-(spiro(benzo[b]thiophene-3(2H),4'-piperidin)-1'-yl)pentyl)benzamide hydrochloride

209349-47-3

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Basic information

Product Name: N-Methyl-N-(3-phenyl-5-(spiro(benzo[b]thiophene-3(2H),4'-piperidin)-1'-yl)pentyl)benzamide hydrochloride
Synonyms:
CAS NO:209349-47-3
Molecular Formula:
Molecular Weight: 521.167
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: N-Methyl-N-(3-phenyl-5-(spiro(benzo[b]thiophene-3(2H),4'-piperidin)-1'-yl)pentyl)benzamide hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: N-Methyl-N-(3-phenyl-5-(spiro(benzo[b]thiophene-3(2H),4'-piperidin)-1'-yl)pentyl)benzamide hydrochloride(209349-47-3)
EPA Substance Registry System: N-Methyl-N-(3-phenyl-5-(spiro(benzo[b]thiophene-3(2H),4'-piperidin)-1'-yl)pentyl)benzamide hydrochloride(209349-47-3)

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: 209349-47-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 209349-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,3,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 209349-47:
(8*2)+(7*0)+(6*9)+(5*3)+(4*4)+(3*9)+(2*4)+(1*7)=143
143 % 10 = 3
So 209349-47-3 is a valid CAS Registry Number.

209349-47-3Upstream product

209350-29-8 N-(5-hydroxy-3-phenylpentyl)-N-methylbenzamide

209349-47-3Downstream Products

209349-47-3Relevant academic research and scientific papers

SPIRO-SUBSTITUTED AZACYCLES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

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, (2008/06/13)

The present invention is directed to spiro-substituted azacycles of the Formula 1: STR1 (wherein R 1, l, m, Q, W, X, Y, and Z are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-1, CCR-2, CCR-2A, CCR-2B, CCR-3, CCR-4, CCR-5, CXCR-3, and/or CXCR-4.

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