Cas 1407150-72-4,2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate

1407150-72-4

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Basic information

Product Name: 2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate
Synonyms: 2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate
CAS NO:1407150-72-4
Molecular Formula:
Molecular Weight: 473.879
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: 2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate(1407150-72-4)
EPA Substance Registry System: 2,2,2-trifluoroethyl 2-[(E)-3-(4-chlorophenyl)-N-phenylacrylamido]-2-phenylacetate(1407150-72-4)

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: 1407150-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1407150-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,1,5 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1407150-72:
(9*1)+(8*4)+(7*0)+(6*7)+(5*1)+(4*5)+(3*0)+(2*7)+(1*2)=124
124 % 10 = 4
So 1407150-72-4 is a valid CAS Registry Number.

1407150-72-4Upstream product

75-89-8 2,2,2-trifluoroethanol

1407150-72-4Downstream Products

1407150-72-4Relevant academic research and scientific papers

A facile and efficient synthesis of 2,2,2-trifluoroethyl 2-[(E)-N-phenylcinnamamido]-2-phenylacetates in trifluoroethanol via sequential Ugi four-component reaction/esterification

Balalaie, Saeed,Motaghedi, Hassan,Bararjanian, Morteza,Bijanzadeh, Hamid Reza,Tahmassebi, Daryoush

, p. 6177 - 6181,5 (2012)

We describe an efficient approach for the synthesis of N-substituted 2-alkenylamides in trifluoroethanol via an Ugi 4-component reaction in short reaction times. The use of a catalytic amount of sulfuric acid in trifluoroethanol gave the desired trifluoroethyl derivatives in good to high yields.

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