Cas 924622-22-0,N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one

924622-22-0

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Basic information

Product Name: N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one
Synonyms: N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one
CAS NO:924622-22-0
Molecular Formula:
Molecular Weight: 429.474
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: N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one(924622-22-0)
EPA Substance Registry System: N-[(diethoxyphosphoryl)methyl]-3-methoxy-4-(phenylthio)-4-(3-oxobut-1-yl)azetidin-2-one(924622-22-0)

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: 924622-22-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 924622-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,6,2 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 924622-22:
(8*9)+(7*2)+(6*4)+(5*6)+(4*2)+(3*2)+(2*2)+(1*2)=160
160 % 10 = 0
So 924622-22-0 is a valid CAS Registry Number.

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924622-22-0Relevant academic research and scientific papers

Highly selective double chalcogenation of isocyanides with disulfide-diselenide mixed systems

Tsuchii, Kaname,Tsuboi, Yasunori,Kawaguchi, Shin-Ichi,Takahashi, Junko,Sonoda, Noboru,Nomoto, Akihiro,Ogawa, Akiya

, p. 415 - 423 (2007/10/03)

A highly selective method for introducing thio and seleno groups into a variety of isocyanides has been developed based on the elucidation of the relative reactivities of organic dichalcogenides and chalcogen-centered free radicals. When the reactions of

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