Cas 1045795-17-2,methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate

1045795-17-2

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Basic information

Product Name: methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate
Synonyms: methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate
CAS NO:1045795-17-2
Molecular Formula:
Molecular Weight: 591.612
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 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate(1045795-17-2)
EPA Substance Registry System: methyl 5-acetamido-4,7,8,9-tetra-O-acetyl-2,6-anhydro-3,5-dideoxy-2-C-(3-phenylprop-2-enyl)-D-erythro-L-gluco-nonoate(1045795-17-2)

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: 1045795-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1045795-17-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,5,7,9 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1045795-17:
(9*1)+(8*0)+(7*4)+(6*5)+(5*7)+(4*9)+(3*5)+(2*1)+(1*7)=162
162 % 10 = 2
So 1045795-17-2 is a valid CAS Registry Number.

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1045795-17-2Relevant academic research and scientific papers

Cross metathesis for the synthesis of novel C-sialosides

Meinke, Sebastian,Thiem, Joachim

, p. 1824 - 1829 (2008)

Cross metathesis of both anomers of C-allyl sialoside (3α/3β) with styrene catalyzed by the second generation Grubbs or Hoveyda-Grubbs catalysts gave the corresponding aryl derivatives (4α/4β) in virtually quantitative yields. The products were hydrogenat

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