Cas 698372-49-5,O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester

698372-49-5

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Basic information

Product Name: O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester
Synonyms: O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester
CAS NO:698372-49-5
Molecular Formula:
Molecular Weight: 684.743
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: O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester(698372-49-5)
EPA Substance Registry System: O-(3,4,6-tri-O-benzyl-2-deoxy-2-nitro-β-D-galactopyranosyl)-N-(benzoyl)-L-serine methyl ester(698372-49-5)

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: 698372-49-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 698372-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 698372-49:
(8*6)+(7*9)+(6*8)+(5*3)+(4*7)+(3*2)+(2*4)+(1*9)=225
225 % 10 = 5
So 698372-49-5 is a valid CAS Registry Number.

698372-49-5Upstream product

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698372-49-5Relevant academic research and scientific papers

2-Nitro thioglycoside donors: Versatile precursors of β-D-glycosides of aminosugars

Barroca, Nadine,Schmidt, Richard R.

, p. 1551 - 1554 (2007/10/03)

2-Nitro thioglycosides can be prepared by the Michael addition of thiophenol to 2-nitroglycal derivatives. NIS/TMSOTf activation of these 2-nitro thioglycosides, in the presence of alcohols, rapidly and cleanly led to the desired glycosides in good yield

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