Cas 1030632-19-9,phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside

1030632-19-9

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Basic information

Product Name: phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside
Synonyms: phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside
CAS NO:1030632-19-9
Molecular Formula:
Molecular Weight: 497.502
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: phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside(1030632-19-9)
EPA Substance Registry System: phenylmethyl 3-O-(p-nitrobenzoyl)-4-O-[(2R,6R)-5,6-dihydro-6-methyl-5-oxo-2H-pyran-2-yl]-β-D-olivopyranoside(1030632-19-9)

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: 1030632-19-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1030632-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,6,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1030632-19:
(9*1)+(8*0)+(7*3)+(6*0)+(5*6)+(4*3)+(3*2)+(2*1)+(1*9)=89
89 % 10 = 9
So 1030632-19-9 is a valid CAS Registry Number.

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1030632-19-9Relevant academic research and scientific papers

De novo synthesis of the trisaccharide subunit of landomycins A and E

Zhou, Maoquan,O'Doherty, George A.

supporting information; experimental part, p. 2283 - 2286 (2009/05/11)

(Chemical Equation Presented) A highly enantio- and diastereoselective synthesis of α-L-rhodinose, β-D-olivose as well as the trisaccharide portion of landomycin A from achiral acetyl furan has been developed. The key transformations include the palladium

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