Cas 858342-80-0,(4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole

858342-80-0

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Basic information

Product Name: (4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole
Synonyms: (4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole
CAS NO:858342-80-0
Molecular Formula:
Molecular Weight: 442.312
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: (4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole(858342-80-0)
EPA Substance Registry System: (4S,5R)-1-(4-bromophenyl)-4,5-dihydro-4-ethyl-5-(oxazolidin-2-one-3-carbonyl)-3-phenyl-1H-pyrazole(858342-80-0)

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: 858342-80-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 858342-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,3,4 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 858342-80:
(8*8)+(7*5)+(6*8)+(5*3)+(4*4)+(3*2)+(2*8)+(1*0)=200
200 % 10 = 0
So 858342-80-0 is a valid CAS Registry Number.

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858342-80-0Relevant academic research and scientific papers

An entry to a chiral dihydropyrazole scaffold: Enantioselective [3 + 2] cycloaddition of nitrile imines

Sibi, Mukund P.,Stanley, Levi M.,Jasperse, Craig P.

, p. 8276 - 8277 (2007/10/03)

We have developed a versatile strategy to access dihydropyrazoles in highly enantioenriched form. Dipolar cycloaddition of electron-deficient acceptors and in situ-generated nitrile imines proceeds with high regio- and enantioselectivity using 10 mol % chiral Lewis acid catalyst. A variety of dihydropyrazoles that incorporate functionality for further manipulation have been prepared. Copyright

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