Cas 1380195-73-2,(R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate

1380195-73-2

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Basic information

Product Name: (R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate
Synonyms: (R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate
CAS NO:1380195-73-2
Molecular Formula:
Molecular Weight: 502.567
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: (R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate(1380195-73-2)
EPA Substance Registry System: (R)-tert-butyl 5-methoxy-3-((R)-2-nitro-1-(p-tolyl)ethyl)-2-oxo-3-phenylindoline-1-carboxylate(1380195-73-2)

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: 1380195-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1380195-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,1,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1380195-73:
(9*1)+(8*3)+(7*8)+(6*0)+(5*1)+(4*9)+(3*5)+(2*7)+(1*3)=162
162 % 10 = 2
So 1380195-73-2 is a valid CAS Registry Number.

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1380195-73-2Relevant academic research and scientific papers

Asymmetric michael addition of N-Boc-protected oxindoles to nitroalkenes catalyzed by a chiral secondary amine

Wang, Chuan,Yang, Xuena,Enders, Dieter

supporting information; experimental part, p. 4832 - 4835 (2012/05/20)

New mission for prolinol ethers: A secondary-amine-catalyzed Michael addition of N-Boc-protected oxindoles to nitroalkenes through a Bronsted base activation mode has been developed, furnishing the products in excellent yields (88-98%), diastereoselectivi

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