Cas 203176-73-2,Phenoxy-acetic acid (3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-phenoxy-acetoxy)-tetrahydro-pyran-3-yl ester

203176-73-2

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Basic information

Product Name: Phenoxy-acetic acid (3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-phenoxy-acetoxy)-tetrahydro-pyran-3-yl ester
Synonyms:
CAS NO:203176-73-2
Molecular Formula:
Molecular Weight: 718.8
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: Phenoxy-acetic acid (3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-phenoxy-acetoxy)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phenoxy-acetic acid (3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-phenoxy-acetoxy)-tetrahydro-pyran-3-yl ester(203176-73-2)
EPA Substance Registry System: Phenoxy-acetic acid (3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-phenoxy-acetoxy)-tetrahydro-pyran-3-yl ester(203176-73-2)

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: 203176-73-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 203176-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,1,7 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 203176-73:
(8*2)+(7*0)+(6*3)+(5*1)+(4*7)+(3*6)+(2*7)+(1*3)=102
102 % 10 = 2
So 203176-73-2 is a valid CAS Registry Number.

203176-73-2Upstream product

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203176-73-2Relevant academic research and scientific papers

Oligosaccharide synthesis on controlled-pore glass as solid phase material

Heckel, Alexander,Mross, Elmar,Jung, Karl-Heinz,Rademann, J?rg,Schmidt, Richard R.

, p. 171 - 173 (1998)

Mercaptopropyl-functionalized controlled-pore glass (MP-CPG, 2) was employed as a solid phase material for the synthesis of α(1-2)-connected trimannoside 16. As a glycosyl donor O-(3,4,6-tri-O-benzyl-2-O-phenoxyacetyl-α-D-mannopyranosyl) trichloroacetimid

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