Cas 460363-29-5,2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid

460363-29-5

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Basic information

Product Name: 2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid
Synonyms: 2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid;2-[(2,4-dimethoxyphenyl)amino]-3-pyridinecarboxylic acid;2-[(2,4-dimethoxyphenyl)amino]nicotinic acid
CAS NO:460363-29-5
Molecular Formula: C14H14N2O4
Molecular Weight: 274.28
EINECS: N/A
Product Categories: N/A
Mol File: 460363-29-5.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid(460363-29-5)
EPA Substance Registry System: 2-[(2,4-dimethoxyphenyl)amino]pyridine-3-carboxylic acid(460363-29-5)

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: 460363-29-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 460363-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,3,6 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 460363-29:
(8*4)+(7*6)+(6*0)+(5*3)+(4*6)+(3*3)+(2*2)+(1*9)=135
135 % 10 = 5
So 460363-29-5 is a valid CAS Registry Number.

460363-29-5Upstream product

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460363-29-5Relevant academic research and scientific papers

Synthesis and mechanistic aspects of 2-anilinonicotinyl-pyrazolo[1,5-a]pyrimidine conjugates that regulate cell proliferation in MCF-7 cells via estrogen signaling

Kamal, Ahmed,Faazil, Shaikh,Hussaini, S.M. Ali,Ramaiah, M. Janaki,Balakrishna,Patel, Nibedita,Pushpavalli,Pal-Bhadra, Manika

, p. 2077 - 2083 (2016)

A series of anilinonicotinyl linked pyrazolo[1,5-a]pyrimidine conjugates (6a-x) were synthesized and evaluated for their antiproliferative activity. Some of these conjugates exhibited promising cytotoxic effects in the MCF-7 cell line and among these 6a a

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