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1462951-15-0

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1462951-15-0 Usage

Molecular structure

1-methyl-7-[4-nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane is a complex organic compound with a spirocyclic structure, consisting of a diazaspiro nonane ring system, a methyl group, and a nitro-substituted phenyl group.

Ether linkage

The presence of a propan-2-yloxy group on the phenyl ring indicates the presence of an ether linkage in the compound.

Biological activity

Due to its complex structure and the presence of the nitro and dialkylamino groups, 1-methyl-7-[4-nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane may exhibit biological activity, making it potentially useful in medicinal chemistry.

Synthesis and characterization

The synthesis and characterization of this compound are of interest to researchers in the field of organic chemistry and drug development, as understanding its properties and behavior can contribute to the development of new pharmaceuticals.

Potential applications

Given its complex structure and possible biological activity, 1-methyl-7-[4-nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane may have potential applications in the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1462951-15-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,6,2,9,5 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1462951-15:
(9*1)+(8*4)+(7*6)+(6*2)+(5*9)+(4*5)+(3*1)+(2*1)+(1*5)=170
170 % 10 = 0
So 1462951-15-0 is a valid CAS Registry Number.

1462951-15-0Relevant articles and documents

NOVEL THIENOPYRIMIDINE DERIVATIVES, PROCESSES FOR THE PREPARATION THEREOF AND THERAPEUTIC USES THEREOF

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Paragraph 0583, (2013/10/08)

The present invention relates to compounds of formula (I): wherein R6 is —CONH2 or a —C(Rα)(Rβ)(OH) group; R is a substituted phenyl or heteroaryl group; R7 is an optionally substituted aryl or heteroaryl group. Process for the preparation thereof and therapeutic use thereof.

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