Cas 911030-80-3,Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester

911030-80-3

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Basic information

Product Name: Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester
Synonyms: Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester
CAS NO:911030-80-3
Molecular Formula:
Molecular Weight: 437.557
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: Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester(911030-80-3)
EPA Substance Registry System: Benzenesulfonic acid (E)-(1R,2S)-1-isopropyl-5-((S)-4-isopropyl-2-oxo-oxazolidin-3-yl)-2,4-dimethyl-5-oxo-pent-3-enyl ester(911030-80-3)

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: 911030-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 911030-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,0,3 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 911030-80:
(8*9)+(7*1)+(6*1)+(5*0)+(4*3)+(3*0)+(2*8)+(1*0)=113
113 % 10 = 3
So 911030-80-3 is a valid CAS Registry Number.

911030-80-3Upstream product

911030-80-3Downstream Products

911030-80-3Relevant academic research and scientific papers

The first total synthesis and structural determination of lagunamycin

Hosokawa, Seijiro,Kuroda, Shoichi,Imamura, Keisuke,Tatsuta, Kuniaki

, p. 6183 - 6186 (2006)

Lagunamycin (1) has been synthesized by using our developed remote stereoinduction, Knorr condensation, periodinane oxidation, and diazonation. This enantioselective synthesis determined the absolute configuration of lagunamycin. Existence of rotational c

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