Catalog No.:AA003NZC

98437-24-2 | Benzofuran-2-boronic acid

Name: Name:Benzofuran-2-boronic acid
Brand: AABLOCKS
SKU: AA003NZC
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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003NZC

Chemical Name:

Benzofuran-2-boronic acid

CAS Number:

98437-24-2

Molecular Formula:

C8H7BO3

Molecular Weight:

161.9504

MDL Number:

MFCD00236019

SMILES:

OB(c1cc2c(o1)cccc2)O

Properties

BP:

340.4 °C at 760 mmHg

Form:

Solid

MP:

114-116 °C(lit.)

Storage:

-20 ℃;Inert atmosphere;

Computed Properties

Complexity:

162

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

Downstream Synthesis Route

98437-24-2

210345-56-5

224321-54-4

[1]Fukuda,Yasumichi;Furuta,Hirosuke;Kusama,Yoshie;Ebisu,Hiroyuki;Oomori,Yasuo;Terashima,Shiro[JournalofMedicinalChemistry,1999,vol.42,#8,p.1448-1458]

98437-24-2

1122-91-4

53348-90-6

[1]Wu,Guo-Jie;Han,Fu-She;Zhao,Yu-Long[RSCAdvances,2015,vol.5,#85,p.69776-69781]

[2]Kondolff,Isabelle;Doucet,Henri;Santelli,Maurice[JournalofHeterocyclicChemistry,2008,vol.45,#1,p.109-118]

[3]Öhberg;Westman[Synlett,2001,#12,p.1893-1896]

[4]Wilson,NoelS.;Sarko,ChristopherR.;Roth,GregoryP.[OrganicProcessResearchandDevelopment,2004,vol.8,#3,p.535-538]

[5]Shore,Gjergji;Morin,Sylvie;Organ,MichaelG.[AngewandteChemie-InternationalEdition,2006,vol.45,#17,p.2761-2766]

[6]Marinozzi,Maura;Carotti,Andrea;Sansone,Emanuele;MacChiarulo,Antonio;Rosatelli,Emiliano;Sardella,Roccaldo;Natalini,Benedetto;Rizzo,Giovanni;Adorini,Luciano;Passeri,Daniela;DeFranco,Francesca;Pruzanski,Mark;Pellicciari,Roberto[BioorganicandMedicinalChemistry,2012,vol.20,#11,p.3429-3445]

98437-24-2

928-90-5

5-benzofuran-2-yl-hex-5-en-1-ol

[1]Oh,ChangHo;Jung,HyungHoon;Kim,KiSeong;Kim,Nakjoong[AngewandteChemie-InternationalEdition,2003,vol.42,#7,p.805-808]

924-44-7

98437-24-2

201230-82-2

39959-51-8

benzofuran-2-yl-(1-oxo-1,3-dihydro-isoindol-2-yl)-aceticacidethylester

[1]TetrahedronLetters,2003,vol.44,p.9017-9019

98437-24-2

76334-36-6

730952-29-1

[1]Shu,Chao;Mega,RiccardoS.;Andreassen,BjörnJ.;Noble,Adam;Aggarwal,VarinderK.[AngewandteChemie-InternationalEdition,2018,vol.57,#47,p.15430-15434][Angew.Chem.,2018,vol.57,p.15656-15660,5]

[2]Huang,Qinhua;Fazio,Alessia;Dai,Guangxiu;Campo,MarinoA.;Larock,RichardC.[JournaloftheAmericanChemicalSociety,2004,vol.126,#24,p.7460-7461]

[3]Luo,Wenping;Yang,Yi;Fang,Yewen;Zhang,Xinxin;Jin,Xiaoping;Zhao,Guicai;Zhang,Li;Li,Yan;Zhou,Wanli;Xia,Tingting;Chen,Bin[AdvancedSynthesisandCatalysis,2019,vol.361,#18,p.4215-4221]

Literature

Title: Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors.

Journal: The Journal of organic chemistry 20111104

Title: Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase.

Journal: Journal of medicinal chemistry 20081127

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