Cas 1609077-44-2,(S)-methyl-2-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate

1609077-44-2

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Basic information

Product Name: (S)-methyl-2-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate
Synonyms: (S)-methyl-2-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate
CAS NO:1609077-44-2
Molecular Formula:
Molecular Weight: 410.47
EINECS: N/A
Product Categories: N/A
Mol File: 1609077-44-2.mol
Article Data: 1

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-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-methyl-2-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate(1609077-44-2)
EPA Substance Registry System: (S)-methyl-2-((S)-3-((tert-butoxycarbonyl)amino)-1-methyl-2-oxoindolin-3-yl)-2-phenylacetate(1609077-44-2)

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: 1609077-44-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609077-44-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,0,7 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1609077-44:
(9*1)+(8*6)+(7*0)+(6*9)+(5*0)+(4*7)+(3*7)+(2*4)+(1*4)=172
172 % 10 = 2
So 1609077-44-2 is a valid CAS Registry Number.

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1609077-44-2Relevant articles and documents

Organocatalyzed enantioselective mannich reaction of pyrazoleamides with isatin-derived ketimines

Li, Tian-Ze,Wang, Xi-Bo,Sha, Feng,Wu, Xin-Yan

, p. 4332 - 4339 (2014/06/09)

The first organocatalytic enantioselective Mannich reaction of pyrazoleamides with isatin-derived N-Boc ketimines has been developed to afford 2-oxindole-based chiral β-amino amides in good yields (84-97%) with excellent diastereo- and enantioselectivitie

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