Cas 73679-59-1,ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside

73679-59-1

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Basic information

Product Name: ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside
Synonyms: ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside
CAS NO:73679-59-1
Molecular Formula:
Molecular Weight: 430.587
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: ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside(73679-59-1)
EPA Substance Registry System: ethyl 2,3,4-trideoxy-2,4-di-C-methyl-6-O-(triphenylmethyl)-α-D-arabino-hexopyranoside(73679-59-1)

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: 73679-59-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73679-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73679-59:
(7*7)+(6*3)+(5*6)+(4*7)+(3*9)+(2*5)+(1*9)=171
171 % 10 = 1
So 73679-59-1 is a valid CAS Registry Number.

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73679-59-1Relevant academic research and scientific papers

Synthetic Routes to 6,8-Dioxabicyclooctyl Pheromones from D-Glucose Derivatives. 4. Synthesis of (-)-α-Multistriatin

Plaumann, Dieter E.,Fitzsimmons, Brian J,Ritchie, Brian M.,Fraser-Reid, Bert

, p. 941 - 946 (2007/10/02)

The precursor for (-)-α-multistriatin (alkyl 2,3,4-trideoxy-2,4-di-C-methyl-α-D-lyxo-hexopyranoside) may be approached from the corresponding isomeric 4-oxo-2-C-methyl- or 2-oxo-4-C-methylpyranosides by (a) methylenation followed by (b) hydrogenation.The

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