Cas 330999-91-2,(3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide

330999-91-2

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Basic information

Product Name: (3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide
Synonyms: (3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide
CAS NO:330999-91-2
Molecular Formula:
Molecular Weight: 482.598
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: (3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide(330999-91-2)
EPA Substance Registry System: (3R,4S,5S)-3,4,5-Tris-benzyloxy-2-methoxy-tetrahydro-thiopyran 1,1-dioxide(330999-91-2)

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: 330999-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 330999-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,9,9 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 330999-91:
(8*3)+(7*3)+(6*0)+(5*9)+(4*9)+(3*9)+(2*9)+(1*1)=172
172 % 10 = 2
So 330999-91-2 is a valid CAS Registry Number.

330999-91-2Upstream product

330999-89-8 methyl 2,3,4-tri-O-benzyl-5-thio-D-xylopyranoside

330999-91-2Downstream Products

330999-93-4 C₂₇H₂₇ClO₄

330999-91-2Relevant academic research and scientific papers

The synthesis of polyoxygenated, enantiopure cyclopentene derivatives using the Ramberg-B?cklund rearrangement

McAllister, Graeme D.,Taylor, Richard J.K.

, p. 1197 - 1200 (2007/10/03)

A novel approach to polyoxygenated enantiopure cyclopentenes, α-chlorocyclopentenones and cyclopentenones is described which utilizes the Ramberg-Ba?cklund rearrangement of thiosugar-derived sulfones. A formal synthesis of the natural aminocyclopentitol, trehazolamine is also reported.

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