Cas 328088-07-9,p-tert-butylphenyl 4-[1-(2-bromobenzyl)-1,1-bis(methoxycarbonyl)methyl]-6-O-(tert-butyldimethylsilyl)-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranoside

328088-07-9

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Basic information

Product Name: p-tert-butylphenyl 4-[1-(2-bromobenzyl)-1,1-bis(methoxycarbonyl)methyl]-6-O-(tert-butyldimethylsilyl)-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranoside
Synonyms:
CAS NO:328088-07-9
Molecular Formula:
Molecular Weight: 675.732
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-tert-butylphenyl 4-[1-(2-bromobenzyl)-1,1-bis(methoxycarbonyl)methyl]-6-O-(tert-butyldimethylsilyl)-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-tert-butylphenyl 4-[1-(2-bromobenzyl)-1,1-bis(methoxycarbonyl)methyl]-6-O-(tert-butyldimethylsilyl)-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranoside(328088-07-9)
EPA Substance Registry System: p-tert-butylphenyl 4-[1-(2-bromobenzyl)-1,1-bis(methoxycarbonyl)methyl]-6-O-(tert-butyldimethylsilyl)-2,3,4-trideoxy-α-D-erythro-hex-2-enopyranoside(328088-07-9)

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: 328088-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 328088-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,0,8 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 328088-07:
(8*3)+(7*2)+(6*8)+(5*0)+(4*8)+(3*8)+(2*0)+(1*7)=149
149 % 10 = 9
So 328088-07-9 is a valid CAS Registry Number.

328088-07-9Upstream product

201233-05-8 p-tert-Butylphenyl 6-O-(tert-butyldimethylsilyl)-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside

328088-07-9Downstream Products

328088-07-9Relevant academic research and scientific papers

Palladium-mediated cyclization on carbohydrate templates synthesis of enantiopure annelated tricyclic compounds

Sinou,Bedjeguelal

, p. 4071 - 4077 (2007/10/03)

Various bromo unsaturated carbohydrates 2-4 have been prepared from ethyl and aryl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside by deacetylation, followed firstly by monosilylation with TBDMSCl and then by alkylation with 2-bromobenzyl brom

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