Cas 760987-52-8,1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol

760987-52-8

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Basic information

Product Name: 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol
Synonyms: 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol
CAS NO:760987-52-8
Molecular Formula:
Molecular Weight: 582.694
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: 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol(760987-52-8)
EPA Substance Registry System: 1,5-anhydro-3-O-benzyl-6-O-(3,4-dimethoxyphenyl)benzyl-2-deoxy-4-O-(4-methoxybenzyl)-D-arabinohex-1-enitol(760987-52-8)

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: 760987-52-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 760987-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,0,9,8 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 760987-52:
(8*7)+(7*6)+(6*0)+(5*9)+(4*8)+(3*7)+(2*5)+(1*2)=208
208 % 10 = 8
So 760987-52-8 is a valid CAS Registry Number.

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760987-52-8Relevant academic research and scientific papers

A Suzuki-Miyaura coupling mediated deprotection as key to the synthesis of a fully lipidated malarial GPI disaccharide

Liu, Xinyu,Seeberger, Peter H.

, p. 1708 - 1709 (2007/10/03)

Ligandless palladium-catalyzed Suzuki-Miyaura coupling converted an inert p-bromobenzyl ether to a DDQ-labile p-(3,4-dimethoxyphenyl) benzyl ether in the presence of azide functionality and this strategy serves as a key step for the convergent synthesis of a fully lipidated malaria GPI disaccharide.

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