Cas 243849-46-9,(2R,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester

243849-46-9

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Basic information

Product Name: (2R,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester
Synonyms: (2R,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester
CAS NO:243849-46-9
Molecular Formula:
Molecular Weight: 386.512
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,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester(243849-46-9)
EPA Substance Registry System: (2R,3R,4S)-(4-benzyloxy-3-methyl-6-phenylsulfanyl-tetrahydropyran-2-yl)-acetic acid methyl ester(243849-46-9)

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: 243849-46-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 243849-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,8,4 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 243849-46:
(8*2)+(7*4)+(6*3)+(5*8)+(4*4)+(3*9)+(2*4)+(1*6)=159
159 % 10 = 9
So 243849-46-9 is a valid CAS Registry Number.

243849-46-9Upstream product

243849-46-9Downstream Products

243849-46-9Relevant academic research and scientific papers

Synthesis of the C29-C37 segment of spongistatin 1

Dunkel, Ralf,Treu, Jens,Martin,Hoffmann

, p. 1539 - 1549 (1999)

Starting from racemic 2α-methyl-8-oxabicyclo[3.2.1]oct-6-en-3-one the spongistatin E segment has been prepared in nine steps (2.3 steps per stereogenic center) with umpolung of anomeric reactivity at C37. This 3,5- syndiol sequence completes our methodolo

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