Cas 181112-82-3,Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester

181112-82-3

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Basic information

Product Name: Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester
Synonyms:
CAS NO:181112-82-3
Molecular Formula:
Molecular Weight: 742.777
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: Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester(CAS DataBase Reference)
NIST Chemistry Reference: Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester(181112-82-3)
EPA Substance Registry System: Succinic acid mono-{(2S,3R,4S,5S,6R)-3-acetoxy-5-benzoyloxy-6-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-2-methoxy-tetrahydro-pyran-4-yl} ester(181112-82-3)

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: 181112-82-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181112-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,1,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 181112-82:
(8*1)+(7*8)+(6*1)+(5*1)+(4*1)+(3*2)+(2*8)+(1*2)=103
103 % 10 = 3
So 181112-82-3 is a valid CAS Registry Number.

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181112-82-3Relevant academic research and scientific papers

Solid phase synthesis of oligosaccharides

Adinolfi, Matteo,Barone, Gaspare,De Napoli, Lorenzo,Iadonisi, Alfonso,Piccialli, Gennaro

, p. 5007 - 5010 (2007/10/03)

An efficient and stereocontrolled solid-phase chemical synthesis of oligosaccarides using a new type of insoluble support (a copolymer of polyethylene glycol and polystyrene) is described. Several Lewis acids were tested as activators of the trichloroacetimidate 12, used as glycosyl donor, in the dimer 13 formation.

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