Cas 1068441-77-9,dimethyl 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate

1068441-77-9

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Basic information

Product Name: dimethyl 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate
Synonyms: dimethyl 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate
CAS NO:1068441-77-9
Molecular Formula:
Molecular Weight: 534.633
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 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate(1068441-77-9)
EPA Substance Registry System: dimethyl 7-allyl-3-tosyl-6,7,10,13-tetrahydro-5H-7,13-diazacyclodeca[a]indene-8,9-dicarboxylate(1068441-77-9)

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: 1068441-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1068441-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,8,4,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1068441-77:
(9*1)+(8*0)+(7*6)+(6*8)+(5*4)+(4*4)+(3*1)+(2*7)+(1*7)=159
159 % 10 = 9
So 1068441-77-9 is a valid CAS Registry Number.

1068441-77-9Upstream product

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1068441-77-9Relevant 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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