Cas 150034-35-8,(2S,4R)-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-4-[(p-toluenesulfonyloxy)methyl]-1,3-dioxolane

150034-35-8

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Basic information

Product Name: (2S,4R)-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-4-[(p-toluenesulfonyloxy)methyl]-1,3-dioxolane
Synonyms:
CAS NO:150034-35-8
Molecular Formula:
Molecular Weight: 476.981
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: (2S,4R)-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-4-[(p-toluenesulfonyloxy)methyl]-1,3-dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4R)-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-4-[(p-toluenesulfonyloxy)methyl]-1,3-dioxolane(150034-35-8)
EPA Substance Registry System: (2S,4R)-2-[2-(4-chlorophenyl)ethyl]-2-[(1H-imidazol-1-yl)methyl]-4-[(p-toluenesulfonyloxy)methyl]-1,3-dioxolane(150034-35-8)

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: 150034-35-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 150034-35-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,0,3 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 150034-35:
(8*1)+(7*5)+(6*0)+(5*0)+(4*3)+(3*4)+(2*3)+(1*5)=78
78 % 10 = 8
So 150034-35-8 is a valid CAS Registry Number.

150034-35-8Upstream product

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150034-35-8Relevant academic research and scientific papers

Synthesis and evaluation of azalanstat analogues as heme oxygenase inhibitors

Vlahakis, Jason Z.,Kinobe, Robert T.,Bowers, Raymond J.,Brien, James F.,Nakatsu, Kanji,Szarek, Walter A.

, p. 1457 - 1461 (2005)

Several analogues based on the lead structure of azalanstat were synthesized and evaluated as novel inhibitors of heme oxygenase (HO). A number of these compounds, which are structurally distinct from metalloporphyrin HO inhibitors, were found to be selec

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