Cas 213611-72-4,[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

213611-72-4

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Basic information

Product Name: [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine
Synonyms: [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine
CAS NO:213611-72-4
Molecular Formula:
Molecular Weight: 508.679
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: [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine(CAS DataBase Reference)
NIST Chemistry Reference: [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine(213611-72-4)
EPA Substance Registry System: [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine(213611-72-4)

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: 213611-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213611-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,6,1 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213611-72:
(8*2)+(7*1)+(6*3)+(5*6)+(4*1)+(3*1)+(2*7)+(1*2)=94
94 % 10 = 4
So 213611-72-4 is a valid CAS Registry Number.

213611-72-4Upstream product

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213611-72-4Relevant academic research and scientific papers

A new route to the asymmetric synthesis of (-)-malyngolide and (-)-epi- malyngolide using N-sulfonyl-l,3-oxazolidines as chiral auxiliaries

Winter, Eric,Hoppe, Dieter

, p. 10329 - 10338 (2007/10/03)

(-)-Malyngolide (1), an antibiotically active δ-lactone, and its epimer 10 were prepared enantioselectively using [2R,2(1S),4R]- and [2R,2(1R),4R]- 4-ethyl-3-(2-nitrobenzenesulfonyl)-2-(1-nonyl-2-oxocyclopentyl)-1,3- oxazolidine (5a and 5b) as key-interme

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