Cas 1387007-73-9,1-(4-fluorophenyl)-1H-benzo[f]chromen-3(2H)-one

1387007-73-9

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Basic information

Product Name: 1-(4-fluorophenyl)-1H-benzo[f]chromen-3(2H)-one
Synonyms:
CAS NO:1387007-73-9
Molecular Formula:
Molecular Weight: 292.309
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: 1-(4-fluorophenyl)-1H-benzo[f]chromen-3(2H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-fluorophenyl)-1H-benzo[f]chromen-3(2H)-one(1387007-73-9)
EPA Substance Registry System: 1-(4-fluorophenyl)-1H-benzo[f]chromen-3(2H)-one(1387007-73-9)

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: 1387007-73-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1387007-73-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,7,0,0 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1387007-73:
(9*1)+(8*3)+(7*8)+(6*7)+(5*0)+(4*0)+(3*7)+(2*7)+(1*3)=169
169 % 10 = 9
So 1387007-73-9 is a valid CAS Registry Number.

1387007-73-9Upstream product

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1387007-73-9Relevant academic research and scientific papers

A novel method for the synthesis of tetrahydrobenzo[a]-xanthen-11-one derivatives using cerium(III) chloride as a highly efficient catalyst

Kidwai, Mazaahir,Jahan, Anwar,Mishra, Neeraj Kumar

, p. 324 - 330 (2012)

Cerium(III) chloride is found to be an highly efficient catalyst for the addition of aldehydes, β-naphthol and cyclic 1,3-dicarbonyl compounds/Meldrum's acid via a multicomponent reaction. The easy availability of starting materials, novel and eco-friendl

One-pot three-component condensation of β-naphthol with arylaldehydes and Meldrum's acid: Synthesis of 1-aryl-1,2-dihydro-benzo[f]chromen-3-ones

Mehrabi, Hossein,Najafian-Ashrafi, Faezeh,Ranjbar-Karimi, Reza

, p. 250 - 252 (2017/06/20)

An efficient and simple method for the synthesis of 1-aryl-1,2-dihydro-benzo[f]chromen-3-ones via a one-pot three-component reaction of β-naphthol, arylaldehydes and Meldrum's acid with Et3N as a base in CH3CN under reflux is reporte

Organocatalytic synthesis of enantioenriched β-arylsplitomicins

Wang, Ji-Yu,Zhang, Hui,Liao, Yu-Hua,Yuan, Wei-Cheng,Feng, Yu-Jun,Zhang, Xiao-Mei

supporting information; experimental part, p. 796 - 800 (2012/07/01)

By employing a chiral bifunctional thiourea-tertiary amine as catalyst, domino Michael-type Friedel-Crafts alkylation/cyclization of -naphthols with akylidene Meldrum's acids was realized. The reactions afforded various enantioenriched -arylsplitomicins with good yields (up to 99%) in moderate enantioselectivities (up to 79%). Georg Thieme Verlag Stuttgart · New York.

A simple and green approach for the synthesis of tetrahydrobenzo[a]- xanthen-11-one derivatives using tetrabutyl ammonium fluoride in water

Gao, Shijay,Tsai, Chen Hsuan,Yao, Ching-Fa

scheme or table, p. 949 - 954 (2009/09/29)

An efficient and simple procedure for the synthesis of 12-aryl- or 12-alkyl-8,9,10,12-tetrahydrobenzo[a]xanfhen-ll-one derivatives has been described. This one-pot multicomponent reaction involves the reaction of aldehydes, 2-naphthol, and cyclic 1,3- dik

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