Cas 960210-69-9,methyl 5-O-(p-methoxybenzyl)-3-S-(4-methylphenyl)-3-thio-β-D-xylofuranoside

960210-69-9

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Basic information

Product Name: methyl 5-O-(p-methoxybenzyl)-3-S-(4-methylphenyl)-3-thio-β-D-xylofuranoside
Synonyms:
CAS NO:960210-69-9
Molecular Formula:
Molecular Weight: 390.5
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: methyl 5-O-(p-methoxybenzyl)-3-S-(4-methylphenyl)-3-thio-β-D-xylofuranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-O-(p-methoxybenzyl)-3-S-(4-methylphenyl)-3-thio-β-D-xylofuranoside(960210-69-9)
EPA Substance Registry System: methyl 5-O-(p-methoxybenzyl)-3-S-(4-methylphenyl)-3-thio-β-D-xylofuranoside(960210-69-9)

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: 960210-69-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960210-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,2,1 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 960210-69:
(8*9)+(7*6)+(6*0)+(5*2)+(4*1)+(3*0)+(2*6)+(1*9)=149
149 % 10 = 9
So 960210-69-9 is a valid CAS Registry Number.

960210-69-9Upstream product

106-45-6 para-thiocresol

960210-69-9Downstream Products

960210-69-9Relevant academic research and scientific papers

Diastereoselective Michael initiated ring closure on vinyl sulfone-modified carbohydrates: A stereospecific and general route to α-substituted cyclopropanes

Das, Indrajit,Pal, Tarun K.,Pathak, Tanmaya

, p. 9181 - 9189 (2007)

(Chemical Equation Presented) Suitably designed vinyl sulfone-modified furanosides act as substrates for Michael initiated ring closure reactions yielding cyclopropanated carbohydrates. The strategy is general in nature and gives access to cyclopropanes w

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