Cas 568588-59-0,(1S,2S)-2-((S)-4-Phenyl-4,5-dihydro-oxazol-2-yl)-cyclohexanecarboxylic acid ((S)-2-hydroxy-1-phenyl-ethyl)-amide

568588-59-0

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Basic information

Product Name: (1S,2S)-2-((S)-4-Phenyl-4,5-dihydro-oxazol-2-yl)-cyclohexanecarboxylic acid ((S)-2-hydroxy-1-phenyl-ethyl)-amide
Synonyms:
CAS NO:568588-59-0
Molecular Formula:
Molecular Weight: 392.498
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: (1S,2S)-2-((S)-4-Phenyl-4,5-dihydro-oxazol-2-yl)-cyclohexanecarboxylic acid ((S)-2-hydroxy-1-phenyl-ethyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S)-2-((S)-4-Phenyl-4,5-dihydro-oxazol-2-yl)-cyclohexanecarboxylic acid ((S)-2-hydroxy-1-phenyl-ethyl)-amide(568588-59-0)
EPA Substance Registry System: (1S,2S)-2-((S)-4-Phenyl-4,5-dihydro-oxazol-2-yl)-cyclohexanecarboxylic acid ((S)-2-hydroxy-1-phenyl-ethyl)-amide(568588-59-0)

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: 568588-59-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 568588-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,8,5,8 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 568588-59:
(8*5)+(7*6)+(6*8)+(5*5)+(4*8)+(3*8)+(2*5)+(1*9)=230
230 % 10 = 0
So 568588-59-0 is a valid CAS Registry Number.

568588-59-0Upstream product

568588-59-0Downstream Products

568588-45-4 (S,S)-1,2-bis[(S)-(4-phenyl)-1,3-oxazolin-2-yl]cyclohexane

568588-59-0Relevant academic research and scientific papers

Asymmetric cyclization-carbonylation of 2-propargyl-1,3-dione

Kato, Keisuke,Tanaka, Maki,Yamamura, Shigeo,Yamamoto, Yasuhiro,Akita, Hiroyuki

, p. 3089 - 3092 (2007/10/03)

The first example of asymmetric cyclization-carbonylation of 2-propargyl-1,3-dione 1 catalyzed by palladium(II) with chiral bisoxazolines (C.H.-BOX) was investigated. The use of bulky alcohols increased the ee of the products 2. The product 2d was converted into bicyclic enones 7 and 8, a useful intermediate for the synthesis of natural products.

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