Cas 1255761-84-2,3,9-dimethoxycarbonyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-1H-pyrrolo[2,3-e]pyrazine]

1255761-84-2

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Basic information

Product Name: 3,9-dimethoxycarbonyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-1H-pyrrolo[2,3-e]pyrazine]
Synonyms:
CAS NO:1255761-84-2
Molecular Formula:
Molecular Weight: 547.573
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: 3,9-dimethoxycarbonyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-1H-pyrrolo[2,3-e]pyrazine](CAS DataBase Reference)
NIST Chemistry Reference: 3,9-dimethoxycarbonyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-1H-pyrrolo[2,3-e]pyrazine](1255761-84-2)
EPA Substance Registry System: 3,9-dimethoxycarbonyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-1H-pyrrolo[2,3-e]pyrazine](1255761-84-2)

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: 1255761-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255761-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,7,6 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1255761-84:
(9*1)+(8*2)+(7*5)+(6*5)+(5*7)+(4*6)+(3*1)+(2*8)+(1*4)=172
172 % 10 = 2
So 1255761-84-2 is a valid CAS Registry Number.

1255761-84-2Upstream product

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1255761-84-2Relevant academic research and scientific papers

Study of reactivity in the 1,3-dipolar cycloaddition reactions leading to new triazolopyrrolopyrazine ring systems

Lauria, Antonino,Guarcello, Annalisa,Dattolo, Gaetano,Almerico, Anna Maria

scheme or table, p. 2067 - 2070 (2010/10/03)

The influence of the structural symmetry of the 2 double-reactive-sites component in the 1,3-dipolar cycloaddition reactions, involving nitrilimines as dipoles, was investigated. The experimental data showed that the loss of the symmetry leads to the form

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