Cas 783323-45-5,(4S,5R)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one

783323-45-5

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Basic information

Product Name: (4S,5R)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one
Synonyms: (4S,5R)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one
CAS NO:783323-45-5
Molecular Formula:
Molecular Weight: 364.488
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)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one(783323-45-5)
EPA Substance Registry System: (4S,5R)-1,5-Dimethyl-3-((R)-2-methyl-5-phenyl-pentanoyl)-4-phenyl-imidazolidin-2-one(783323-45-5)

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: 783323-45-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 783323-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,3,2 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 783323-45:
(8*7)+(7*8)+(6*3)+(5*3)+(4*2)+(3*3)+(2*4)+(1*5)=175
175 % 10 = 5
So 783323-45-5 is a valid CAS Registry Number.

783323-45-5Upstream product

783323-45-5Downstream Products

783323-45-5Relevant academic research and scientific papers

Enantioselective synthesis of (R)-2-methylalkanoic acids: A convenient approach to α-substituted chiral carboxylic acid derivatives

Shirali, Shyam,Zhang, Aijun

, p. 3435 - 3441 (2007/10/03)

Racemization-free deacylation of N-acylimidazolidine-2-ones using lithium hydroperoxide affords the corresponding α-substituted chiral carboxylic acids in high yield while permitting recovery of the chiral auxiliary.

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