Cas 1448459-90-2,(S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate

1448459-90-2

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Basic information

Product Name: (S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate
Synonyms: (S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate
CAS NO:1448459-90-2
Molecular Formula:
Molecular Weight: 478.548
EINECS: N/A
Product Categories: N/A

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: (S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate(1448459-90-2)
EPA Substance Registry System: (S)-methyl 2-acetamido-3-(2-(bis(4-methoxybenzyl)amino)pyrimidin-5-yl)propanoate(1448459-90-2)

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: 1448459-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1448459-90-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,4,5 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1448459-90:
(9*1)+(8*4)+(7*4)+(6*8)+(5*4)+(4*5)+(3*9)+(2*9)+(1*0)=202
202 % 10 = 2
So 1448459-90-2 is a valid CAS Registry Number.

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1448459-90-2Downstream Products

1448459-90-2Relevant academic research and scientific papers

Asymmetric synthesis of aminopyrimidine and cyclic guanidine amino acids

M?schwitzer, Vicki D.,Kariuki, Benson M.,Redman, James E.

supporting information, p. 4526 - 4528 (2013/08/23)

Syntheses of amino acids with aminopyrimidine and cyclic guanidine side chains are described. The synthetic route employed Heck coupling of methyl 2-acetamidoacrylate to 4-methoxybenzyl protected 2-amino-5-iodopyrimidine, followed by Rh(I)-catalyzed asymm

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