Cas 905266-84-4,p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside

905266-84-4

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Basic information

Product Name: p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
Synonyms: p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
CAS NO:905266-84-4
Molecular Formula:
Molecular Weight: 617.838
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: p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(905266-84-4)
EPA Substance Registry System: p-tolyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(905266-84-4)

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: 905266-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905266-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,2,6 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 905266-84:
(8*9)+(7*0)+(6*5)+(5*2)+(4*6)+(3*6)+(2*8)+(1*4)=174
174 % 10 = 4
So 905266-84-4 is a valid CAS Registry Number.

905266-84-4Upstream product

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905266-84-4Relevant academic research and scientific papers

Iterative one-pot syntheses of chitotetroses

Huang, Lijun,Wang, Zhen,Li, Xiaoning,Ye, Xin-shan,Huang, Xuefei

, p. 1669 - 1679 (2006)

Rapid syntheses of chitotetrose derivatives were achieved in good yields using the newly developed reactivity independent iterative one-pot strategy. The protective groups on donors and acceptors were independently evaluated allowing matching of the two p

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