Cas 1337534-57-2,(S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol

1337534-57-2

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Basic information

Product Name: (S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol
Synonyms: (S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol
CAS NO:1337534-57-2
Molecular Formula:
Molecular Weight: 300.281
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: (S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol(1337534-57-2)
EPA Substance Registry System: (S)-3-(4,5-dimethyl-3-oxido-1H-imidazol-1-yl)-1,1,1-trifluoro-2-phenylpropan-2-ol(1337534-57-2)

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: 1337534-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1337534-57-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,7,5,3 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1337534-57:
(9*1)+(8*3)+(7*3)+(6*7)+(5*5)+(4*3)+(3*4)+(2*5)+(1*7)=162
162 % 10 = 2
So 1337534-57-2 is a valid CAS Registry Number.

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1337534-57-2Relevant academic research and scientific papers

New β-amino-α-trifluoromethyl alcohols and their exploration in the synthesis of trifluoromethylated imidazole derivatives

Mlostoń, Grzegorz,Obijalska, Emilia,Heimgartner, Heinz

, p. 951 - 955 (2011)

Racemic and enantiomerically pure β-amino-α-trifluoromethyl alcohols were obtained via sequential nucleophilic trifluoromethylation of selected α-imino ketones, derived from arylglyoxals, and subsequent removal of the MeO or Ph(Me)CH substituent, respecti

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