Cas 574002-69-0,1H-Pyrrole-2-carboxamide, N-[(2E)-3-[2-amino-1-(triphenylmethyl)-1H-imidazol-4-yl]-2-propenyl]-4, 5-dibromo-1-methyl-

574002-69-0

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Basic information

Product Name: 1H-Pyrrole-2-carboxamide, N-[(2E)-3-[2-amino-1-(triphenylmethyl)-1H-imidazol-4-yl]-2-propenyl]-4, 5-dibromo-1-methyl-
Synonyms:
CAS NO:574002-69-0
Molecular Formula: C31H27Br2N5O
Molecular Weight: 645.396
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: 1H-Pyrrole-2-carboxamide, N-[(2E)-3-[2-amino-1-(triphenylmethyl)-1H-imidazol-4-yl]-2-propenyl]-4, 5-dibromo-1-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrrole-2-carboxamide, N-[(2E)-3-[2-amino-1-(triphenylmethyl)-1H-imidazol-4-yl]-2-propenyl]-4, 5-dibromo-1-methyl-(574002-69-0)
EPA Substance Registry System: 1H-Pyrrole-2-carboxamide, N-[(2E)-3-[2-amino-1-(triphenylmethyl)-1H-imidazol-4-yl]-2-propenyl]-4, 5-dibromo-1-methyl-(574002-69-0)

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: 574002-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 574002-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,4,0,0 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 574002-69:
(8*5)+(7*7)+(6*4)+(5*0)+(4*0)+(3*2)+(2*6)+(1*9)=140
140 % 10 = 0
So 574002-69-0 is a valid CAS Registry Number.

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574002-69-0Relevant academic research and scientific papers

Synthesis of the pyrrole-imidazole alkaloid sventrin from the marine sponge Agelas sventres

Breckle, Gregor,Polborn, Kurt,Lindel, Thomas

, p. 451 - 456 (2007/10/03)

The marine pyrrole-imidazole alkaloid sventrin (1) and the hitherto unknown dehydrooroidin (3) have been synthesized stereoselectively via alkyne intermediates. The pathways start from a 2-azido-4-alkynylimidazole which can be chemo- and stereoselectively

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