Cas 1352050-95-3,(E)-3-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one

1352050-95-3

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Basic information

Product Name: (E)-3-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one
Synonyms: (E)-3-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one
CAS NO:1352050-95-3
Molecular Formula:
Molecular Weight: 382.41
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-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one(1352050-95-3)
EPA Substance Registry System: (E)-3-(3,4-difluorophenyl)-1-4-[(E)-3-phenyl-2-propenoyl]piperazino-2-propen-1-one(1352050-95-3)

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: 1352050-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352050-95-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,5 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1352050-95:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*5)+(3*0)+(2*9)+(1*5)=123
123 % 10 = 3
So 1352050-95-3 is a valid CAS Registry Number.

1352050-95-3Upstream product

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1352050-95-3Relevant academic research and scientific papers

Synthesis of cinnamide dimers as potential antibacterial and antifungal agents

Kamal, Ahmed,Ramakrishna,Raju,Subba Rao,Joseph, Joveeta,Siddhardha,Murty

, p. 957 - 965 (2012/07/01)

A series of new cinnamide dimers was synthesized (5a-6a) and evaluated for th e i r antimicrobial and antifungal activity. All the compounds investigated have shown significant antimicrobial a c t iv i ty against gram-positive and gram-negative bacterial

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