Cas 182509-75-7,(3aS,4R,7S,7aR)-3-((S)-3-Hydroxy-5-methyl-hex-4-enoyl)-4,8,8-trimethyl-1-phenyl-octahydro-4,7-methano-benzoimidazol-2-one

182509-75-7

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Basic information

Product Name: (3aS,4R,7S,7aR)-3-((S)-3-Hydroxy-5-methyl-hex-4-enoyl)-4,8,8-trimethyl-1-phenyl-octahydro-4,7-methano-benzoimidazol-2-one
Synonyms:
CAS NO:182509-75-7
Molecular Formula:
Molecular Weight: 396.53
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: (3aS,4R,7S,7aR)-3-((S)-3-Hydroxy-5-methyl-hex-4-enoyl)-4,8,8-trimethyl-1-phenyl-octahydro-4,7-methano-benzoimidazol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,7S,7aR)-3-((S)-3-Hydroxy-5-methyl-hex-4-enoyl)-4,8,8-trimethyl-1-phenyl-octahydro-4,7-methano-benzoimidazol-2-one(182509-75-7)
EPA Substance Registry System: (3aS,4R,7S,7aR)-3-((S)-3-Hydroxy-5-methyl-hex-4-enoyl)-4,8,8-trimethyl-1-phenyl-octahydro-4,7-methano-benzoimidazol-2-one(182509-75-7)

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: 182509-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 182509-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,5,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 182509-75:
(8*1)+(7*8)+(6*2)+(5*5)+(4*0)+(3*9)+(2*7)+(1*5)=147
147 % 10 = 7
So 182509-75-7 is a valid CAS Registry Number.

182509-75-7Upstream product

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182509-75-7Relevant academic research and scientific papers

New chiral acetate imide enolate for stereoselective aldol reactions

Palomo, Claudio,Oiarbide, Mikel,Gonzalez, Alberto,Garcia, Jesus M.,Berree, Fabienne,Linden, Anthony

, p. 6931 - 6934 (2007/10/03)

The chiral imide acetate 4 reacts upon lithium and titanium enolate formation conditions with aldehydes in a stereoselective manner. Remarkably, aldols obtained from aromatic and α,β-unsaturated aldehydes exhibited opposite stereochemistry than those obtained from aliphatic aldehydes.

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