Cas 65252-65-5,6β-((<i>R</i>)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ<sup>4</sup>-penicillanic acid

65252-65-5

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Basic information

Product Name: 6β-((R)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ⁴-penicillanic acid
Synonyms: 6β-((R)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ⁴-penicillanic acid
CAS NO:65252-65-5
Molecular Formula:
Molecular Weight: 405.475
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: 6β-((R)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ⁴-penicillanic acid(CAS DataBase Reference)
NIST Chemistry Reference: 6β-((R)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ⁴-penicillanic acid(65252-65-5)
EPA Substance Registry System: 6β-((R)-2,2-dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-1β-oxo-1λ⁴-penicillanic acid(65252-65-5)

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: 65252-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 65252-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,5 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65252-65:
(7*6)+(6*5)+(5*2)+(4*5)+(3*2)+(2*6)+(1*5)=125
125 % 10 = 5
So 65252-65-5 is a valid CAS Registry Number.

65252-65-5Upstream product

3511-16-8 hetacillin

65252-65-5Downstream Products

65252-65-5Relevant academic research and scientific papers

Hetacillin (R)- and (S)-sulfoxides. Synthesis and structure-activity relationships

Gottestein,Kim,Shih,McGregor

, p. 240 - 242 (2007/10/10)

Hetacillin was oxidized with m-chloroperbenzoic acid to give the corresponding (R)- and (S)-sulfoxides. Ozonization of hetacillin not only oxidized the sulfide but caused unexpected oxidation of the imidazolidine ring to a 2H-imidazoline. The biological s

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