Cas 1333260-15-3,(3aS,8bS)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole salt with N-tosyl-(R)-phenylglycine

1333260-15-3

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Basic information

Product Name: (3aS,8bS)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole salt with N-tosyl-(R)-phenylglycine
Synonyms:
CAS NO:1333260-15-3
Molecular Formula:
Molecular Weight: 464.585
EINECS: N/A
Product Categories: N/A
Mol File: 1333260-15-3.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: (3aS,8bS)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole salt with N-tosyl-(R)-phenylglycine(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,8bS)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole salt with N-tosyl-(R)-phenylglycine(1333260-15-3)
EPA Substance Registry System: (3aS,8bS)-1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole salt with N-tosyl-(R)-phenylglycine(1333260-15-3)

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: 1333260-15-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333260-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,6 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1333260-15:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*6)+(3*0)+(2*1)+(1*5)=113
113 % 10 = 3
So 1333260-15-3 is a valid CAS Registry Number.

1333260-15-3Upstream product

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1333260-15-3Relevant articles and documents

Resolution of 1,2,3,3a,4,8b-hexahydrocyclopenta[b]indole via diastereomeric salt formation with N-Tosyl-(R)-phenylglycine

Higashijima, Shinji,Inoue, Yukiko,Maehashi, Takaya,Miura, Hidetoshi,Kubota, Yasuhiro,Funabiki, Kazumasa,Matsui, Masaki

supporting information; scheme or table, p. 968 - 969 (2011/01/07)

Enantiopure l,2,3,3a,4,8b-hexahydrocyclopenta[b]indole, the starting material of indoline dyes, could be obtained from the diastereomeric salt with N-tosyl-(R)-phenylglycine in ethanol.

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