Cas 1200-98-2,1-methoxy-1-(2-methylphenyl)propan-2-one

1200-98-2

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Basic information

Product Name: 1-methoxy-1-(2-methylphenyl)propan-2-one
Synonyms: 1-methoxy-1-(2-methylphenyl)propan-2-one
CAS NO:1200-98-2
Molecular Formula:
Molecular Weight: 178.231
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-methoxy-1-(2-methylphenyl)propan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-methoxy-1-(2-methylphenyl)propan-2-one(1200-98-2)
EPA Substance Registry System: 1-methoxy-1-(2-methylphenyl)propan-2-one(1200-98-2)

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: 1200-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1200-98-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1200-98:
(6*1)+(5*2)+(4*0)+(3*0)+(2*9)+(1*8)=42
42 % 10 = 2
So 1200-98-2 is a valid CAS Registry Number.

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1200-98-2Downstream Products

1200-98-2Relevant academic research and scientific papers

α-Methoxyketone Synthesis via Ketone Homologation: ZrCl4-Mediated Hydroxy Sulfone Rearrangements

Montana, John G.,Phillipson, Neil,Taylor, Richard J. K.

, p. 2289 - 2290 (1994)

The adducts between ketones and the anion derived from benzene undergo efficient, regioselective rearrangement to give α-methoxyketones when treated with ZrCl4 and HfCl4; this new procedure allows the sulfone-mediated homologation

Ketone homologation to produce α-methoxyketones: Application to conduritol synthesis

Phillipson, Neil,Anson, Michael S.,Montana, John G.,Taylor, Richard J. K.

, p. 2821 - 2829 (2007/10/03)

The scope of Trost's sulfone homologation procedure for the conversion of ketones into their α-methoxylated higher homologues has been dramatically expanded. The use of zirconium (or hafnium) tetrachloride in the hydroxy sulfone rearrangement step gives g

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