Cas 1312082-17-9,N-((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-nitrotetrahydro-2H-pyran-2-yl)acetamide

1312082-17-9

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Basic information

Product Name: N-((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-nitrotetrahydro-2H-pyran-2-yl)acetamide
Synonyms:
CAS NO:1312082-17-9
Molecular Formula:
Molecular Weight: 520.582
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: N-((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-nitrotetrahydro-2H-pyran-2-yl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-nitrotetrahydro-2H-pyran-2-yl)acetamide(1312082-17-9)
EPA Substance Registry System: N-((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-3-nitrotetrahydro-2H-pyran-2-yl)acetamide(1312082-17-9)

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: 1312082-17-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312082-17-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,0,8 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1312082-17:
(9*1)+(8*3)+(7*1)+(6*2)+(5*0)+(4*8)+(3*2)+(2*1)+(1*7)=99
99 % 10 = 9
So 1312082-17-9 is a valid CAS Registry Number.

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1312082-17-9Relevant academic research and scientific papers

Acetyl chloride - Silver nitrate - Acetonitrile: A reagent system for the synthesis of 2-nitroglycals and 2-nitro-1-acetamido sugars from glycals

Kancharla, Pavan K.,Reddy, Y. Suman,Dharuman, Suresh,Vankar, Yashwant D.

, p. 5832 - 5837 (2011)

A new reagent system comprising acetyl chloride, silver nitrate, and acetonitrile has been developed for the synthesis of 2-nitroglycals from the corresponding glycals. Under certain conditions, the formation of 2-nitro-1-acetamido sugars has also been observed. In addition, a few other non-carbohydrate-derived olefins also gave the corrresponding conjugated nitroolefins.

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