Cas 1255761-89-7,3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine]

1255761-89-7

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Basic information

Product Name: 3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine]
Synonyms: 3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine]
CAS NO:1255761-89-7
Molecular Formula:
Molecular Weight: 515.574
EINECS: N/A
Product Categories: N/A
Mol File: 1255761-89-7.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: 3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine](CAS DataBase Reference)
NIST Chemistry Reference: 3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine](1255761-89-7)
EPA Substance Registry System: 3,9-diacetyl-1,6,11-triphenyl-[1,11,11a,11b-tetrahydrobis-1,2,4-triazolo[3,4-c:4',3'-a]-3H-pyrrolo[2,3-e]pyrazine](1255761-89-7)

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: 1255761-89-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255761-89-7 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 1255761-89:
(9*1)+(8*2)+(7*5)+(6*5)+(5*7)+(4*6)+(3*1)+(2*8)+(1*9)=177
177 % 10 = 7
So 1255761-89-7 is a valid CAS Registry Number.

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1255761-89-7Relevant articles and documents

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

supporting information; experimental part, 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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