Cas 219533-80-9,1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one

219533-80-9

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Basic information

Product Name: 1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one
Synonyms: 1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one
CAS NO:219533-80-9
Molecular Formula:
Molecular Weight: 378.513
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: 1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one(219533-80-9)
EPA Substance Registry System: 1-(4-Methoxy-phenyl)-2-methyl-3-methylsulfanyl-3-(toluene-4-sulfonyl)-propan-1-one(219533-80-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 219533-80-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 219533-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 219533-80:
(8*2)+(7*1)+(6*9)+(5*5)+(4*3)+(3*3)+(2*8)+(1*0)=139
139 % 10 = 9
So 219533-80-9 is a valid CAS Registry Number.

219533-80-9Upstream product

219533-80-9Downstream Products

219533-87-6 (E)-1-(4-Methoxy-phenyl)-2-methyl-3-(toluene-4-sulfonyl)-propenone

219533-80-9Relevant academic research and scientific papers

Novel photochemical addition of aromatic aldehydes to ketene dithioacetal S,S-dioxides and its application to organic synthesis

Ogura, Katsuyuki,Arai, Takayuki,Kayano, Akio,Akazome, Motohiro

, p. 9051 - 9054 (2007/10/03)

On irradiation (>290 nm) in the absence or presence of benzophenone, various aromatic aldehydes add to ketene dithioacetal S,S-dioxides to give the corresponding 1:1 adducts, which were shown to be synthetic precursors of indanone derivatives.

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