Cas 1036637-37-2,methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate

1036637-37-2

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Basic information

Product Name: methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate
Synonyms: methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate
CAS NO:1036637-37-2
Molecular Formula:
Molecular Weight: 429.473
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: methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate(1036637-37-2)
EPA Substance Registry System: methyl 4-((3-[(tert-butoxycarbonyl)amino]phenyl)amino)-2-nitro-4-phenylbutanoate(1036637-37-2)

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: 1036637-37-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1036637-37-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,6,3 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1036637-37:
(9*1)+(8*0)+(7*3)+(6*6)+(5*6)+(4*3)+(3*7)+(2*3)+(1*7)=142
142 % 10 = 2
So 1036637-37-2 is a valid CAS Registry Number.

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1036637-37-2Relevant academic research and scientific papers

A mild procedure for the Lewis acid-catalyzed ring-opening of activated cyclopropanes with amine nucleophiles

Lifchits, Olga,Charette, Andre B.

, p. 2809 - 2812 (2008)

(Chemical Equation Presented) The Lewis acid-catalyzed ring-opening of methyl 1-nitrocyclopropanecarboxylates with amine nucleophiles is described. The reaction proceeds at room temperature and with complete preservation of the enantiomeric purity from th

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