Cas 393795-21-6,2-Oxazolidinone, 3-[(2S,3R,6E)-8-(acetyloxy)-3-hydroxy-2,6-dimethyl-1-oxo-6-octenyl]-4-( phenylmethyl)-, (4S)-

393795-21-6

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Basic information

Product Name: 2-Oxazolidinone, 3-[(2S,3R,6E)-8-(acetyloxy)-3-hydroxy-2,6-dimethyl-1-oxo-6-octenyl]-4-( phenylmethyl)-, (4S)-
Synonyms:
CAS NO:393795-21-6
Molecular Formula: C22H29NO6
Molecular Weight: 403.475
EINECS: N/A
Product Categories: N/A
Mol File: 393795-21-6.mol
Article Data: 2

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: 2-Oxazolidinone, 3-[(2S,3R,6E)-8-(acetyloxy)-3-hydroxy-2,6-dimethyl-1-oxo-6-octenyl]-4-( phenylmethyl)-, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Oxazolidinone, 3-[(2S,3R,6E)-8-(acetyloxy)-3-hydroxy-2,6-dimethyl-1-oxo-6-octenyl]-4-( phenylmethyl)-, (4S)-(393795-21-6)
EPA Substance Registry System: 2-Oxazolidinone, 3-[(2S,3R,6E)-8-(acetyloxy)-3-hydroxy-2,6-dimethyl-1-oxo-6-octenyl]-4-( phenylmethyl)-, (4S)-(393795-21-6)

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: 393795-21-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 393795-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,3,7,9 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 393795-21:
(8*3)+(7*9)+(6*3)+(5*7)+(4*9)+(3*5)+(2*2)+(1*1)=196
196 % 10 = 6
So 393795-21-6 is a valid CAS Registry Number.

393795-21-6Upstream product

393795-21-6Downstream Products

393795-21-6Relevant articles and documents

An enantioselective synthesis of FR182877 provides a chemical rationalization of its structure and affords multigram quantities of its direct precursor

Vanderwal, Christopher D.,Vosburg, David A.,Weiler, Sven,Sorensen, Erik J.

, p. 5393 - 5407 (2007/10/03)

The evolution of a strategy culminating in an efficient, enantioselective synthesis of the potent microtubule-stabilizing agent FR182877 is described. Guided by a proposed biogenesis of this complex natural product, a solution emerged that involved the fi

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