Cas 1168136-65-9,methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside

1168136-65-9

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Basic information

Product Name: methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside
Synonyms: methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside
CAS NO:1168136-65-9
Molecular Formula:
Molecular Weight: 382.459
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: methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside(1168136-65-9)
EPA Substance Registry System: methyl α-D-3-amino-4,6-O-((R)-benzylidene)-2,3-dideoxy-2-C,3-N-(ethane-1,2-diyl)-3-N-phenylamino-allopyranoside(1168136-65-9)

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: 1168136-65-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1168136-65-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,8,1,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1168136-65:
(9*1)+(8*1)+(7*6)+(6*8)+(5*1)+(4*3)+(3*6)+(2*6)+(1*5)=159
159 % 10 = 9
So 1168136-65-9 is a valid CAS Registry Number.

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1168136-65-9Relevant academic research and scientific papers

Stereoselective synthesis by double reductive amination ring closure of novel aza-heteroannulated sugars

Laventine, Dominic M.,Davies, Michelle,Evinson, Emma L.,Jenkins, Paul R.,Cullis, Paul M.,García, Marcos D.

experimental part, p. 4766 - 4774 (2009/10/09)

We present here the stereoselective synthesis of a series of 2/3-N-pyrrolidine derivatives of glycosides produced by diastereoselective double reductive amination ring closure of 1,4-dicarbonyl compounds. These precursors were produced by tandem ozonolysi

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