Cas 1335129-18-4,(E)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate

1335129-18-4

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Basic information

Product Name: (E)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate
Synonyms: (E)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate
CAS NO:1335129-18-4
Molecular Formula:
Molecular Weight: 397.901
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)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate(1335129-18-4)
EPA Substance Registry System: (E)-3-(2-chlorophenyl)-1-(cyclohexylamino)-3-oxo-1-phenylprop-1-en-2-yl acetate(1335129-18-4)

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: 1335129-18-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1335129-18-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,1,2 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1335129-18:
(9*1)+(8*3)+(7*3)+(6*5)+(5*1)+(4*2)+(3*9)+(2*1)+(1*8)=134
134 % 10 = 4
So 1335129-18-4 is a valid CAS Registry Number.

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1335129-18-4Relevant academic research and scientific papers

Highly stereoselective synthesis of tetrasubstituted alkenes via hydroamination of alkynes and C-H acetoxylation

Liu, Weibing,Chen, Cui,Zhang, Qing

supporting information; experimental part, p. 6484 - 6486 (2011/11/04)

A novel reaction including the sequence of hydroamination of alkynes and subsequent oxidative C-H bond functionalization has been developed in the presence of diacetoxyiodobenzene (DIB). The method allows us to synthesize a wide range of tetrasubstituted

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