Cas 151477-72-4,Pyrido[2,3-d]pyrimidine-2,4-diamine, 5-methyl-6-[[(3,4,5-trichlorophenyl)amino]methyl]-

151477-72-4

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Basic information

Product Name: Pyrido[2,3-d]pyrimidine-2,4-diamine, 5-methyl-6-[[(3,4,5-trichlorophenyl)amino]methyl]-
Synonyms:
CAS NO:151477-72-4
Molecular Formula: C15H13Cl3N6
Molecular Weight: 383.667
EINECS: N/A
Product Categories: N/A
Mol File: 151477-72-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Pyrido[2,3-d]pyrimidine-2,4-diamine, 5-methyl-6-[[(3,4,5-trichlorophenyl)amino]methyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Pyrido[2,3-d]pyrimidine-2,4-diamine, 5-methyl-6-[[(3,4,5-trichlorophenyl)amino]methyl]-(151477-72-4)
EPA Substance Registry System: Pyrido[2,3-d]pyrimidine-2,4-diamine, 5-methyl-6-[[(3,4,5-trichlorophenyl)amino]methyl]-(151477-72-4)

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: 151477-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 151477-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,4,7 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151477-72:
(8*1)+(7*5)+(6*1)+(5*4)+(4*7)+(3*7)+(2*7)+(1*2)=134
134 % 10 = 4
So 151477-72-4 is a valid CAS Registry Number.

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151477-72-4Relevant academic research and scientific papers

Synthesis of 5-methyl-5-deaza nonclassical antifolates as inhibitors of dihydrofolate reductases and as potential antipneumocystis, antitoxoplasma, and antitumor agents

Gangjee,Shi,Queener,Barrows,Kisliuk

, p. 3437 - 3443 (1993)

A series of 2,4-diamino-5-methyl-6-(anilinomethyl)pyrido[2,3- d]pyrimidines 4-9 were synthesized as 5-deaza nonclassical antifolates containing trimethoxy, dichloro-, or trichlorophenyl substitutions and a N- H, N-CH3, or N-CHO at the 10-positi

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