Cas 635316-98-2,(2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol

635316-98-2

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Basic information

Product Name: (2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol
Synonyms: (2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol
CAS NO:635316-98-2
Molecular Formula:
Molecular Weight: 362.398
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: (2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol(635316-98-2)
EPA Substance Registry System: (2R,3S,4S,5S,6R)-3,5-Bis-benzyloxy-2-fluoro-6-hydroxymethyl-tetrahydro-pyran-4-ol(635316-98-2)

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: 635316-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 635316-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,3,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 635316-98:
(8*6)+(7*3)+(6*5)+(5*3)+(4*1)+(3*6)+(2*9)+(1*8)=162
162 % 10 = 2
So 635316-98-2 is a valid CAS Registry Number.

635316-98-2Upstream product

213998-08-4 phenyl 3,6-di-O-acetyl-2,4-di-O-benzyl-1-thio-α-D-mannopyranoside

635316-98-2Downstream Products

635316-98-2Relevant academic research and scientific papers

Synthesis of an octamannosyled glycan chain, the key oligosaccharide structure in ER-associated degradation

Matsuo, Ichiro,Ito, Yukishige

, p. 2163 - 2168 (2003)

The high-mannose type decasaccharide (Man8GlcNAc2), the proposed ligand of ER residing mannosidase-like proteins (MLP), and its monoglycosylated homologue (α-Glc1Man8GlcNAc 2) were synthesized. The oligosaccharide assembly was performed in a convergent and stereoselective manner, using three oligosaccharide components, a core trisaccharide having a β-mannoside bond, a liner mannotriose, and a branched mannotetraose.

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