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Home Imidazoles 6504-13-8
6504-13-8,MFCD00230532
Catalog No.:AA00EJ7L

6504-13-8 | 4-(1H-Benzo[d]imidazol-2-yl)phenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$50.00   $35.00
- +
1g
97%
in stock  
$122.00   $85.00
- +
5g
97%
in stock  
$329.00   $230.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00EJ7L
Chemical Name:
4-(1H-Benzo[d]imidazol-2-yl)phenol
CAS Number:
6504-13-8
Molecular Formula:
C13H10N2O
Molecular Weight:
210.2313
MDL Number:
MFCD00230532
SMILES:
Oc1ccc(cc1)c1nc2c([nH]1)cccc2
Properties
Properties
 
Form:
Solid  
Storage:
Room Temperature;Inert atmosphere;  

Computed Properties
 
Complexity:
238  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
2.9  

Downstream Synthesis Route

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1982,vol.21,p.872-874

[1]LiebigsAnnalenderChemie,1987,p.495-498

[1]Locationinpatent:experimentalpartXu,Hui;Yu,Dong-Hui;Liu,Le-Le;Yan,Peng-Fei;Jia,Li-Wei;Li,Guang-Ming;Yue,Zheng-Yu[JournalofPhysicalChemistryB,2010,vol.114,#1,p.141-150]

[1]Wang,Zhao-Gang;Cao,Xiao-Hua;Yang,Yao;Lu,Ming[SyntheticCommunications,2015,vol.45,#12,p.1476-1483]

[2]Nasseri,MohammadAli;Rezazadeh,Zinat;Kazemnejadi,Milad;Allahresani,Ali[CatalysisLetters,2021,vol.151,#4,p.1049-1067]

[3]Bera,Atanu;Sk,Motahar;Singh,Khushboo;Banerjee,Debasis[ChemicalCommunications,2019,vol.55,#42,p.5958-5961]

[1]ChemistryofHeterocyclicCompounds,2018,vol.54,p.351-354    Khim.Geterotsikl.Soedin.,2018,vol.54,p.351-354,4

Literature

Title: A fluorescent probe for biothiols based on the conjugate addition of thiols to α,β-unsaturated ester.

Journal: Luminescence : the journal of biological and chemical luminescence 20110101

Title: 1H-Benzimidazole derivatives as mammalian DNA topoisomerase I inhibitors.

Journal: Acta biochimica Polonica 20070101

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