Cas 76513-72-9,Acetic acid (1S,2S,6R)-2-acetoxy-6-((2R,4R,5R,6R)-4,5-diacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-cyclohexyl ester

76513-72-9

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Basic information

Product Name: Acetic acid (1S,2S,6R)-2-acetoxy-6-((2R,4R,5R,6R)-4,5-diacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-cyclohexyl ester
Synonyms:
CAS NO:76513-72-9
Molecular Formula:
Molecular Weight: 430.452
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: Acetic acid (1S,2S,6R)-2-acetoxy-6-((2R,4R,5R,6R)-4,5-diacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1S,2S,6R)-2-acetoxy-6-((2R,4R,5R,6R)-4,5-diacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-cyclohexyl ester(76513-72-9)
EPA Substance Registry System: Acetic acid (1S,2S,6R)-2-acetoxy-6-((2R,4R,5R,6R)-4,5-diacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-cyclohexyl ester(76513-72-9)

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: 76513-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76513-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76513-72:
(7*7)+(6*6)+(5*5)+(4*1)+(3*3)+(2*7)+(1*2)=139
139 % 10 = 9
So 76513-72-9 is a valid CAS Registry Number.

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76513-72-9Relevant academic research and scientific papers

Reactions of Relevance to the Chemistry of Aminoglycoside Antibiotics. Part 15. The Selective Modification of Neamine by Radical-induced Deamination

Barton, Derek H. R.,Bringmann, Gerhard,Motherwell, William B.

, p. 2665 - 2669 (2007/10/02)

The reaction of neamine tetraformamide tetra-acetate with phosphorus oxychloride and triethylamine has been studied.Isocyanide formation was found to proceed in stepwise fashion.The radical-induced reduction of the resultant derivatives by tri-n-butylstan

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