Cas 178872-62-3,Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester

178872-62-3

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Basic information

Product Name: Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester
Synonyms: Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester
CAS NO:178872-62-3
Molecular Formula:
Molecular Weight: 614.757
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: Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester(CAS DataBase Reference)
NIST Chemistry Reference: Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester(178872-62-3)
EPA Substance Registry System: Sulfuric acid mono-[6-((2R,3S,4R,5R,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexyl] ester(178872-62-3)

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: 178872-62-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 178872-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,8,7 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 178872-62:
(8*1)+(7*7)+(6*8)+(5*8)+(4*7)+(3*2)+(2*6)+(1*2)=193
193 % 10 = 3
So 178872-62-3 is a valid CAS Registry Number.

178872-62-3Upstream product

178872-62-3Downstream Products

178872-62-3Relevant academic research and scientific papers

Synthesis of sialyl Lewis X analogues

Dekany, Gyula,Wright, Karen,Ward, Peter,Toth, Istvan

, p. 383 - 398 (2007/10/03)

Sialyl Lewis X (SLex) analogs 2a and 2b were synthesised, where the N-acetyl-D-glucose and the D-galactose units of SLex 1 were replaced with an alkyl and a heteroalkyl spacer. Sulphate ester 6i was also synthesised from alcohol 6b and chlorosulphonic acid. A novel promoter, silver mercaptoethanesulphonate, was used to synthesise α-sialosides 2c, 7b and 7c.

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