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[(1R,2S,3S,5S)-8-methyl-3-phenyl-8-azabicyclo[3.2.1]oct-2-yl]methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50372-82-2

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50372-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50372-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,7 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50372-82:
(7*5)+(6*0)+(5*3)+(4*7)+(3*2)+(2*8)+(1*2)=102
102 % 10 = 2
So 50372-82-2 is a valid CAS Registry Number.

50372-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,3S,4S,5R)-8-methyl-3-phenyl-8-azabicyclo[3.2.1]octan-4-yl]methanol

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:50372-82-2 SDS

50372-82-2Upstream product

50372-82-2Relevant academic research and scientific papers

Tropane derivatives and method for their synthesis

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Page column 23, (2010/11/29)

A compound of formula (I) wherein R1-R6have any of the values defined in the specification are described, as well as pharmaceutical compositions comprising a compound of formula (I), and methods for preparing and using compounds of f

Synthesis and biological properties of new 2β-alkyl- and 2β-aryl-3- (substituted phenyl)tropane derivatives: Stereochemical effect of C-3 on affinity and selectivity for neuronal dopamine and serotonin transporters

Kozikowski, Alan P.,Araldi, Gian Luca,Prakash,Zhang, Mei,Johnson, Kenneth M.

, p. 4973 - 4982 (2007/10/03)

In our efforts to identify molecules that might act as cocaine antagonists or cocaine partial agonists, we have been involved in efforts to further elucidate the nature of cocaine's binding to the dopamine transporter (DAT) through strategic modifications

Synthesis, dopamine transporter affinity, dopamine uptake inhibition, and locomotor stimulant activity of 2-substituted 3β-phenyltropane derivatives

Xu, Lifen,Kelkar, Shreekrishna V.,Lomenzo, Stacey A.,Izenwasser, Sari,Katz, Jonathan L.,Kline, Richard H.,Trudell, Mark L.

, p. 858 - 863 (2007/10/03)

A series of 2β-substituted 3β-phenyltropanes were synthesized as analogs of cocaine and tested in vitro for their ability to displace bound [3H]WIN 35,428 (2b) and inhibit dopamine uptake in rat caudate-putamen tissue. The analogs bound with hi

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