Cas 265646-58-0,(S)-4-Phenyl-3-{(E)-3-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-imidazol-4-yl]-acryloyl}-oxazolidin-2-one

265646-58-0

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Basic information

Product Name: (S)-4-Phenyl-3-{(E)-3-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-imidazol-4-yl]-acryloyl}-oxazolidin-2-one
Synonyms:
CAS NO:265646-58-0
Molecular Formula:
Molecular Weight: 465.53
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)-4-Phenyl-3-{(E)-3-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-imidazol-4-yl]-acryloyl}-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-4-Phenyl-3-{(E)-3-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-imidazol-4-yl]-acryloyl}-oxazolidin-2-one(265646-58-0)
EPA Substance Registry System: (S)-4-Phenyl-3-{(E)-3-[1-(2,4,6-trimethyl-benzenesulfonyl)-1H-imidazol-4-yl]-acryloyl}-oxazolidin-2-one(265646-58-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 265646-58-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 265646-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,6,4 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 265646-58:
(8*2)+(7*6)+(6*5)+(5*6)+(4*4)+(3*6)+(2*5)+(1*8)=170
170 % 10 = 0
So 265646-58-0 is a valid CAS Registry Number.

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265646-58-0Relevant academic research and scientific papers

First stereoselective synthesis of an optically pure β-substituted histidine: (2s,3s)-β-methylhistidine

Wang, Sihe,Tang, Xuejun,Hruby, Victor J.

, p. 1307 - 1310 (2000)

We report the first example of the asymmetric synthesis of the β- substituted histidine, (2S,3S)-β-methylhistidine. A key in the synthesis is the use of the protecting group, 2-mesitylenesulfonyl (Mts-), for the imidazole ring to minimize epimerization during synthesis. (C) 2000 Elsevier Science Ltd.

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