Cas 1035140-58-9,(2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester

1035140-58-9

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Basic information

Product Name: (2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester
Synonyms: (2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester
CAS NO:1035140-58-9
Molecular Formula:
Molecular Weight: 593.839
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: (2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester(1035140-58-9)
EPA Substance Registry System: (2S,4S,5R)-4-[2-oxo-3-(2-triisopropyl-silanyloxy-ethyl)-imidazolidine-1-carbonyl]-2,5-diphenyl-pyrrolidine-2-carboxylic acid methyl ester(1035140-58-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1035140-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1035140-58-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,1,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1035140-58:
(9*1)+(8*0)+(7*3)+(6*5)+(5*1)+(4*4)+(3*0)+(2*5)+(1*8)=99
99 % 10 = 9
So 1035140-58-9 is a valid CAS Registry Number.

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1035140-58-9Relevant academic research and scientific papers

Anti-MRSA agent discovery using diversity-oriented synthesis

Thomas, Gemma L.,Spandl, Richard J.,Glansdorp, Freija G.,Welch, Martin,Bender, Andreas,Cockfield, Joshua,Lindsay, Jodi A.,Bryant, Clare,Brown, Derek F. J.,Loiseleur, Olivier,Rudyk, Helene,Ladlow, Mark,Spring, David R.

supporting information; experimental part, p. 2808 - 2812 (2009/02/06)

Beating the superbugs: Diversity-oriented synthesis using a solid-supported phosphonate unit to synthesize 242 drug-like compounds based on 18 natural-productlike scaffolds led to the discovery of gemmacin (see scheme). This new structural class of antibiotic is active towards methicillin-resistant Staphylococcus aureus (MRSA). (Chemical Equation Presented).

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