Cas 1397693-94-5,dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate

1397693-94-5

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Basic information

Product Name: dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate
Synonyms: dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate
CAS NO:1397693-94-5
Molecular Formula:
Molecular Weight: 494.568
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: dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate(1397693-94-5)
EPA Substance Registry System: dimethyl (E)-2-(9-tosyl-1-vinyl-1,3,4,9-tetrahydro-2H-β-carbolin-2-yl)but-2-enedioate(1397693-94-5)

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: 1397693-94-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1397693-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,7,6,9 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1397693-94:
(9*1)+(8*3)+(7*9)+(6*7)+(5*6)+(4*9)+(3*3)+(2*9)+(1*4)=235
235 % 10 = 5
So 1397693-94-5 is a valid CAS Registry Number.

1397693-94-5Upstream product

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1397693-94-5Relevant academic research and scientific papers

Medium-sized and strained heterocycles from non-catalysed and gold-catalysed conversions of β-carbolines

Medina, Sandra,González-Gómez, álvaro,Domínguez, Gema,Pérez-Castells, Javier

experimental part, p. 7167 - 7176 (2012/10/08)

2-Allyl-1-vinyl-β-carbolines and dihydropyrrolo-β-carbolines react with activated internal alkynes through novel rearrangement reactions leading to complex polycyclic structures. Favored reaction pathways depend on reaction conditions and on the presence

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