Cas 1340563-51-0,(S)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one

1340563-51-0

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Basic information

Product Name: (S)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one
Synonyms: (S)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one
CAS NO:1340563-51-0
Molecular Formula:
Molecular Weight: 409.488
EINECS: N/A
Product Categories: N/A
Mol File: 1340563-51-0.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)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one(1340563-51-0)
EPA Substance Registry System: (S)-1-benzyl-6'-methoxy-2',3',4',9'-tetrahydrospiro[indoline-3,1'-pyrido[3,4-b]indol]-2-one(1340563-51-0)

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: 1340563-51-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1340563-51-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,0,5,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1340563-51:
(9*1)+(8*3)+(7*4)+(6*0)+(5*5)+(4*6)+(3*3)+(2*5)+(1*1)=130
130 % 10 = 0
So 1340563-51-0 is a valid CAS Registry Number.

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1340563-51-0Relevant articles and documents

Enantioselective Pictet-Spengler reactions of isatins for the synthesis of spiroindolones

Badillo, Joseph J.,Silva-García, Abel,Shupe, Benjamin H.,Fettinger, James C.,Franz, Annaliese K.

supporting information; experimental part, p. 5550 - 5553 (2011/11/05)

The condensation cyclization between isatins and 5-methoxy tryptamine catalyzed by chiral phosphoric acids provides spirooxindole tetrahydro-β- carboline products in excellent yields (up to 99%) and enantioselectivity (up to 98:2 er). A comparison of cata

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