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2-amino-4-methoxy-N-[8-(4-methoxybenzyl)-8-azabicyclo[3.2.1]oct-3-yl]pyrimidine-5-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76351-85-4

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76351-85-4 Usage

General Description

The chemical 2-amino-4-methoxy-N-[8-(4-methoxybenzyl)-8-azabicyclo[3.2.1]oct-3-yl]pyrimidine-5-carboxamide is a complex organic compound with a pyrimidine base. It contains an amino group, a methoxy group, and a carboxamide group attached to the pyrimidine ring. Additionally, it features a unique azabicyclo[3.2.1]octane ring system with a methoxybenzyl substituent. 2-amino-4-methoxy-N-[8-(4-methoxybenzyl)-8-azabicyclo[3.2.1]oct-3-yl]pyrimidine-5-carboxamide may have potential pharmacological or biological applications due to its complex structure and multiple functional groups. Further research and analysis are needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 76351-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,5 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76351-85:
(7*7)+(6*6)+(5*3)+(4*5)+(3*1)+(2*8)+(1*5)=144
144 % 10 = 4
So 76351-85-4 is a valid CAS Registry Number.

76351-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-methoxy-N-[8-[(4-methoxyphenyl)methyl]-8-azabicyclo[3.2.1]octan-3-yl]pyrimidine-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76351-85-4 SDS

76351-85-4Downstream Products

76351-85-4Relevant 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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