Cas 560132-74-3,2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol

560132-74-3

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Basic information

Product Name: 2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol
Synonyms: 2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol
CAS NO:560132-74-3
Molecular Formula:
Molecular Weight: 344.48
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: 2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol(CAS DataBase Reference)
NIST Chemistry Reference: 2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol(560132-74-3)
EPA Substance Registry System: 2D-(1,5/1,2,3,4)-1-O-acetyl-1,5-anhydro-4-O-[(tert-butyl)dimethylsilyl]-2,3-O-isopropylidenecyclopentane-1,1,2,3,4,5-hexol(560132-74-3)

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: 560132-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 560132-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,0,1,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 560132-74:
(8*5)+(7*6)+(6*0)+(5*1)+(4*3)+(3*2)+(2*7)+(1*4)=123
123 % 10 = 3
So 560132-74-3 is a valid CAS Registry Number.

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560132-74-3Relevant academic research and scientific papers

Cyclopentanes from N-aminoglyconolactams: Reaction mechanism and improved access to diazocyclopentanones

Hu, Guixian,Vasella, Andrea

, p. 2434 - 2446 (2004)

One of the two mechanisms to rationalize the Pb(OAc)4 oxidation of 1 to 2 and 3 postulates the intermediate generation of a carbene 25 via the acetoxy-diazepinone 22 and the oxadiazoline 23 (Scheme 2). This mechanism was excluded on the basis o

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