Cas 1000375-90-5,methyl (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate

1000375-90-5

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Basic information

Product Name: methyl (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate
Synonyms: methyl (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate
CAS NO:1000375-90-5
Molecular Formula:
Molecular Weight: 548.633
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 (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate(1000375-90-5)
EPA Substance Registry System: methyl (allyl 2,3-di-O-benzyl-4-O-p-methoxybenzyl-α-D-galactopyranosid)uronate(1000375-90-5)

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: 1000375-90-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1000375-90-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,3,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000375-90:
(9*1)+(8*0)+(7*0)+(6*0)+(5*3)+(4*7)+(3*5)+(2*9)+(1*0)=85
85 % 10 = 5
So 1000375-90-5 is a valid CAS Registry Number.

1000375-90-5Upstream product

1000375-90-5Downstream Products

1000375-90-5Relevant academic research and scientific papers

Allyl deprotection of galacturonic acid derivatives: mechanistic aspects of mercuric-catalyzed prop-1-enyl acetal cleavage

Barbier, Maximilien,Grand, Eric,Kovensky, Jose

, p. 2635 - 2640 (2007)

Different deallylation methods were assayed for selective deprotection of allyl galactopyranosiduronic acid derivatives. A two-step procedure using DABCO and (Ph3P)3RhCl followed by mercuric-assisted cleavage gave quantitative yields. Reaction in the presence of [18O]water allowed us to obtain evidence about the mechanism of prop-1-enyl cleavage.

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