Cas 147241-10-9,2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide

147241-10-9

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Basic information

Product Name: 2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide
Synonyms: 2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide
CAS NO:147241-10-9
Molecular Formula:
Molecular Weight: 325.249
EINECS: N/A
Product Categories: N/A
Mol File: 147241-10-9.mol
Article Data: 1

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: 2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide(147241-10-9)
EPA Substance Registry System: 2-(3-Bromo-phenyl)-N-methyl-N-(2-pyrrolidin-1-yl-ethyl)-acetamide(147241-10-9)

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: 147241-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147241-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147241-10:
(8*1)+(7*4)+(6*7)+(5*2)+(4*4)+(3*1)+(2*1)+(1*0)=109
109 % 10 = 9
So 147241-10-9 is a valid CAS Registry Number.

147241-10-9Upstream product

147241-10-9Downstream Products

710274-81-0 [2-(3-Bromo-phenyl)-ethyl]-methyl-(2-pyrrolidin-1-yl-ethyl)-amine

147241-10-9Relevant articles and documents

Synthesis and Binding Characteristics of Potential SPECT Imaging Agents for ?-1 and ?-2 Binding Sites

He, Xiao-shu,Bowen, Wayne D.,Lee, Kan Sam,Williams, Wanda,Weinberger, Daniel R.,Costa, Brian R. de

, p. 566 - 571 (1993)

2-, 3-, and 4-iodophenyl derivatives of the high-affinity ? ligand N--N-methyl-2-(1-pyrrolidinyl)ethylamine (1) were synthesized in two to four steps starting from N-methyl-2-(1-pyrrolidinyl)ethylamine.These compounds were eva

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