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2-Amino-N-(8-(o-chlorobenzyl)-3-beta-nortropanyl)-4-methoxy-5-pyrimidi necarboxamide is a complex organic compound with a molecular formula of C18H21ClN4O3. It is a derivative of pyridine carboxamide, featuring a pyrimidine ring and an amino group. The molecule contains an o-chlorobenzyl group attached to the nortropane moiety, which is a structural component of tropane alkaloids. The 4-methoxy group provides additional functionality to the molecule. 2-Amino-N-(8-(o-chlorobenzyl)-3-beta-nortropanyl)-4-methoxy-5-pyrimidi necarboxamide is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. Its specific activity and pharmacological properties are subject to ongoing research, as the structure suggests it may interact with various biological receptors due to its unique combination of functional groups.

84923-35-3

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84923-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84923-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84923-35:
(7*8)+(6*4)+(5*9)+(4*2)+(3*3)+(2*3)+(1*5)=153
153 % 10 = 3
So 84923-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H24ClN5O2/c1-28-19-16(10-23-20(22)25-19)18(27)24-13-8-14-6-7-15(9-13)26(14)11-12-4-2-3-5-17(12)21/h2-5,10,13-15H,6-9,11H2,1H3,(H,24,27)(H2,22,23,25)

84923-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-N-[8-[(2-chlorophenyl)methyl]-8-azabicyclo[3.2.1]octan-3-yl]-4-methoxypyrimidine-5-carboxamide

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

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More Details:84923-35-3 SDS

84923-35-3Downstream Products

84923-35-3Relevant academic research and scientific papers

Studies on the neuroleptic benzamides. III - Synthesis and antidopaminergic properties of new 3-nortropane derivatives

Dostert,Imbert,Langlois,et al.

, p. 105 - 110 (2007/10/02)

Various benzamides prepared from 4-alkoxy pyrimidine 5-carboxylic acids and 3-amino nortropane derivatives have been tested for their potential antipsychotic activity. Two compounds exhibited pharamacological activity equivalent to that of haloperidol but had lower toxicity and lower potency to induced catalepsy. Antidopaminergic activity is observed mainly in compounds in which the nortropane ring is substituted in the equatorial position, having a benzyl substituent on the basic nitrogen. The influence of electron attractor or donor substituents carried by the benzyl ring has been evaluated. Some aspects of structure-activity relationships are discussed.

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