Cas 1197986-24-5,dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate

1197986-24-5

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Basic information

Product Name: dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate
Synonyms: dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate
CAS NO:1197986-24-5
Molecular Formula:
Molecular Weight: 347.291
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: dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate(1197986-24-5)
EPA Substance Registry System: dimethyl 2-(3,3,3-trifluoro-1-(4-methoxyphenylamino)propylidene)malonate(1197986-24-5)

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: 1197986-24-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1197986-24-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,9,8 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1197986-24:
(9*1)+(8*1)+(7*9)+(6*7)+(5*9)+(4*8)+(3*6)+(2*2)+(1*4)=225
225 % 10 = 5
So 1197986-24-5 is a valid CAS Registry Number.

1197986-24-5Upstream product

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1197986-24-5Relevant academic research and scientific papers

Preparations and reactions of 2-trifluoromethylketenimines

Katagiri, Toshimasa,Handa, Michiharu,Asano, Hiroyuki,Asanuma, Teppei,Mori, Tomohiro,Jukurogi, Tatsuya,Uneyama, Kenji

experimental part, p. 714 - 717 (2009/12/25)

Preparations and reactions of a series of 2-trifluoromethylketenimines are described. Trifluoromethylketenimines were prepared from trifluoropropanoic acids via corresponding imidoyl chlorides in good yields. 2-Trifluoromethylketenimine was functionalized

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