Cas 107486-29-3,3-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole

107486-29-3

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Basic information

Product Name: 3-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole
Synonyms: 3-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole
CAS NO:107486-29-3
Molecular Formula:
Molecular Weight: 447.129
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-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole(107486-29-3)
EPA Substance Registry System: 3-Dibromoacetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole(107486-29-3)

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: 107486-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107486-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107486-29:
(8*1)+(7*0)+(6*7)+(5*4)+(4*8)+(3*6)+(2*2)+(1*9)=133
133 % 10 = 3
So 107486-29-3 is a valid CAS Registry Number.

107486-29-3Upstream product

55523-07-4 3-Acetyl-9-methyl-2-phenylimidazo<1,2-a>benzimidazole

107486-29-3Downstream Products

107486-29-3Relevant academic research and scientific papers

STUDIES OF IMIDAZOBENZIMIDAZOLE DERIVATIVES. 21. SYNTHESIS OF HALOKETONES IN THE IMIDAZOBENZIMIDAZOLE SERIES

Anisimova, V. A.,Korochina, T. B.,Avdyunina, N. I.,Simonov, A. M.

, p. 275 - 282 (2007/10/02)

Methods for the synthesis of imidazobenzimidazole haloketone derivatives have been investigated.It has been found that α-bromoketone derivatives of this heterocycle can be prepared either by bromination of 3-acylimidazobenzimidazoles with br

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