Cas 1414838-12-2,(E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate

1414838-12-2

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Basic information

Product Name: (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate
Synonyms: (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate
CAS NO:1414838-12-2
Molecular Formula:
Molecular Weight: 331.292
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: (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate(1414838-12-2)
EPA Substance Registry System: (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-3-[trifluoromethyl]phenyl}acrylate(1414838-12-2)

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: 1414838-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1414838-12-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,8,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1414838-12:
(9*1)+(8*4)+(7*1)+(6*4)+(5*8)+(4*3)+(3*8)+(2*1)+(1*2)=152
152 % 10 = 2
So 1414838-12-2 is a valid CAS Registry Number.

1414838-12-2Upstream product

1414838-12-2Downstream Products

1414838-12-2Relevant academic research and scientific papers

Ruthenium-catalyzed oxidative C-H alkenylation of aryl carbamates

Li, Jie,Kornhaass, Christoph,Ackermann, Lutz

supporting information, p. 11343 - 11345,3 (2012/12/12)

A cationic ruthenium(ii) catalyst enabled highly efficient oxidative alkenylations of electron-rich arenes bearing removable, weakly coordinating carbamates, and allowed for cross-dehydrogenative C-H bond functionalization in an aerobic manner. This journ

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