Cas 338744-52-8,2-(trimethylsilyl)ethyl 2-O-acetyl-4,6-O-benzylidene-3-O-[methyl 4,7,8,9-tetra-O-acetyl-5-(N-acetylacetamido)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate]-β-D-galactopyranoside

338744-52-8

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Basic information

Product Name: 2-(trimethylsilyl)ethyl 2-O-acetyl-4,6-O-benzylidene-3-O-[methyl 4,7,8,9-tetra-O-acetyl-5-(N-acetylacetamido)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate]-β-D-galactopyranoside
Synonyms:
CAS NO:338744-52-8
Molecular Formula:
Molecular Weight: 926.011
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: 2-(trimethylsilyl)ethyl 2-O-acetyl-4,6-O-benzylidene-3-O-[methyl 4,7,8,9-tetra-O-acetyl-5-(N-acetylacetamido)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate]-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-(trimethylsilyl)ethyl 2-O-acetyl-4,6-O-benzylidene-3-O-[methyl 4,7,8,9-tetra-O-acetyl-5-(N-acetylacetamido)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate]-β-D-galactopyranoside(338744-52-8)
EPA Substance Registry System: 2-(trimethylsilyl)ethyl 2-O-acetyl-4,6-O-benzylidene-3-O-[methyl 4,7,8,9-tetra-O-acetyl-5-(N-acetylacetamido)-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulopyranosylonate]-β-D-galactopyranoside(338744-52-8)

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: 338744-52-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 338744-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,7,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 338744-52:
(8*3)+(7*3)+(6*8)+(5*7)+(4*4)+(3*4)+(2*5)+(1*2)=168
168 % 10 = 8
So 338744-52-8 is a valid CAS Registry Number.

338744-52-8Upstream product

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338744-52-8Relevant academic research and scientific papers

A highly convergent synthesis of a complex oligosaccharide derived from group B type III Streptococcus

Demchenko,Boons

, p. 2547 - 2554 (2001)

An efficient synthesis of a heptasaccharide derived from group B type III Streptococcus carrying an artificial spacer (1) is described. Rapid assembly of a protected heptasaccharide (16a) is accomplished from readily available building blocks 2-5 without a single protecting group manipulation between glycosylation steps. The synthetic strategy may be applied to the assembly of other branched complex oligosaccharides. The deprotected heptasaccharide 1 was coupled to a poly[N-(acryloyloxy)succinimide, and the resulting material will be used for the development of an ELISA assay to detect antibodies against GBS, type III in pregnant women.

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