Cas 1219730-41-2,4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine

1219730-41-2

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Basic information

Product Name: 4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine
Synonyms: 4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine
CAS NO:1219730-41-2
Molecular Formula:
Molecular Weight: 373.362
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: 4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine(1219730-41-2)
EPA Substance Registry System: 4-(3-fluorophenyl)-N-(4-fluorophenyl)[1,3]oxazolo[4,5-c]quinolin-2-amine(1219730-41-2)

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: 1219730-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1219730-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,7,3 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1219730-41:
(9*1)+(8*2)+(7*1)+(6*9)+(5*7)+(4*3)+(3*0)+(2*4)+(1*1)=142
142 % 10 = 2
So 1219730-41-2 is a valid CAS Registry Number.

1219730-41-2Upstream product

1219730-18-3 1-(4-fluorophenyl)-3-[2-(3-fluorophenyl)-4-hydroxyquinolin-3-yl]urea

1219730-41-2Downstream Products

1219730-41-2Relevant academic research and scientific papers

New 1,3-oxazolo[4,5-c]quinoline derivatives: Synthesis and evaluation of antibacterial and antituberculosis properties

Eswaran, Sumesh,Adhikari, Airody Vasudeva,Ajay Kumar

experimental part, p. 957 - 966 (2010/04/26)

A new class of fused oxazoloquinoline derivatives was synthesized starting from 2-bromo-1-phenylethanones 1a-b through multi-step reactions. The newly synthesized compounds were evaluated for their in vitro antibacterial against Escherichia coli (ATTC-259

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