Cas 1246745-50-5,(R)-3-(4-trifluoromethoxybenzyl)-1-(3,5-dichlorophenyl)-6-bromo-3-methyl-1H-imidazo[1,2a]imidazole-2-one

1246745-50-5

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Basic information

Product Name: (R)-3-(4-trifluoromethoxybenzyl)-1-(3,5-dichlorophenyl)-6-bromo-3-methyl-1H-imidazo[1,2a]imidazole-2-one
Synonyms:
CAS NO:1246745-50-5
Molecular Formula:
Molecular Weight: 535.147
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: (R)-3-(4-trifluoromethoxybenzyl)-1-(3,5-dichlorophenyl)-6-bromo-3-methyl-1H-imidazo[1,2a]imidazole-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-(4-trifluoromethoxybenzyl)-1-(3,5-dichlorophenyl)-6-bromo-3-methyl-1H-imidazo[1,2a]imidazole-2-one(1246745-50-5)
EPA Substance Registry System: (R)-3-(4-trifluoromethoxybenzyl)-1-(3,5-dichlorophenyl)-6-bromo-3-methyl-1H-imidazo[1,2a]imidazole-2-one(1246745-50-5)

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: 1246745-50-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1246745-50-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,7,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1246745-50:
(9*1)+(8*2)+(7*4)+(6*6)+(5*7)+(4*4)+(3*5)+(2*5)+(1*0)=165
165 % 10 = 5
So 1246745-50-5 is a valid CAS Registry Number.

1246745-50-5Upstream product

688756-17-4 (R)-1-(3,5-dichloro-phenyl)-3-methyl-3-(4-trifluoromethoxy-benzyl)-1H-imidazo[1,2-a]-imidazol-2-one

1246745-50-5Downstream Products

1246745-50-5Relevant academic research and scientific papers

Efficient synthesis of a small molecule, nonpeptide inhibitor of LFA-1

Wang, Xiao-Jun,Xu, Yibo,Zhang, Li,Krishnamurthy, Dhileepkumar,Wirth, Thomas,Nicola, Thomas,Senanayake, Chris H.

scheme or table, p. 4412 - 4415 (2010/12/18)

Figure Presented. A three-stage process for the synthesis of LFA-1 inhibitor 1 from amine 4 with an overall yield of 65% is described. The key stage involves a Ph3PCl2-induced dehydration/cyclization of urea 6 followed by a regiosele

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