Cas 1169769-96-3,(2S)-[2-((3R)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

1169769-96-3

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Basic information

Product Name: (2S)-[2-((3R)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester
Synonyms:
CAS NO:1169769-96-3
Molecular Formula:
Molecular Weight: 366.46
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: (2S)-[2-((3R)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-[2-((3R)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(1169769-96-3)
EPA Substance Registry System: (2S)-[2-((3R)-3-methyl-2-oxo-2,3-dihydro-1H-indol-3-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(1169769-96-3)

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: 1169769-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1169769-96-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,9,7,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1169769-96:
(9*1)+(8*1)+(7*6)+(6*9)+(5*7)+(4*6)+(3*9)+(2*9)+(1*6)=223
223 % 10 = 3
So 1169769-96-3 is a valid CAS Registry Number.

1169769-96-3Upstream product

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1169769-96-3Relevant academic research and scientific papers

A homodinuclear Mn(III)2-Schiff base complex for catalytic asymmetric 1,4-additions of oxindoles to nitroalkenes

Kato, Yuko,Furutachi, Makoto,Chen, Zhihua,Mitsunuma, Harunobu,Matsunaga, Shigeki,Shibasaki, Masakatsu

supporting information; experimental part, p. 9168 - 9169 (2009/12/06)

(Chemical Equation Presented) Catalytic asymmetric 1,4-additions of 3-substituted oxindoles to β-aryl, β-heteroaryl, and β-alkenyl nitroalkenes are described. A new homodinuclear Mn2(OAc) 2-Schiff base 1 complex was required to reali

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