Cas 1295578-49-2,octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside

1295578-49-2

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Basic information

Product Name: octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside
Synonyms: octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside
CAS NO:1295578-49-2
Molecular Formula:
Molecular Weight: 997.537
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: octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside(1295578-49-2)
EPA Substance Registry System: octadecyl 3,4,6-tri-O-benzyl-2-deoxy-2-[(octadecyloxycarbonyl)methyl]-α-D-glucopyranoside(1295578-49-2)

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: 1295578-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1295578-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,5,5,7 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1295578-49:
(9*1)+(8*2)+(7*9)+(6*5)+(5*5)+(4*7)+(3*8)+(2*4)+(1*9)=212
212 % 10 = 2
So 1295578-49-2 is a valid CAS Registry Number.

1295578-49-2Upstream product

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1295578-49-2Relevant academic research and scientific papers

Stereoselective diversity-oriented syntheses of functionalized saccharides from bicyclic carbohydrate 1,2-lactones

Yin, Jian,Linker, Torsten

experimental part, p. 2447 - 2461 (2011/04/26)

Bicyclic carbohydrate 1,2-lactones have been synthesized in only two steps and high yields by saponification and subsequent cyclization from known malonate addition products to glycals. The gluco-configured lactone serves as an important precursor for div

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