Home Other Building Blocks 1079-21-6
1079-21-6,MFCD00002342
Catalog No.:AA003HSR

1079-21-6 | [1,1'-Biphenyl]-2,5-diol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$23.00   $16.00
- +
25g
98%
in stock  
$252.00   $177.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003HSR
Chemical Name:
[1,1'-Biphenyl]-2,5-diol
CAS Number:
1079-21-6
Molecular Formula:
C12H10O2
Molecular Weight:
186.2066
MDL Number:
MFCD00002342
SMILES:
Oc1ccc(c(c1)c1ccccc1)O
NSC Number:
407988
Properties
Properties
 
BP:
383°C at 760 mmHg  
Form:
Solid  
MP:
98-100 °C(lit.);  
Refractive Index:
1.6010 (estimate)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
175  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
3.2  

Downstream Synthesis Route

[1]Abe[BulletinoftheChemicalSocietyofJapan,1943,vol.18,p.93,96]

885-77-8    1079-21-6   
4-(di-p-tolylmethyl)-1,1’-biphenyl-2,5-diol 

[1]Singh,Pallavi;Singh,UdaiPratap;Peddinti,RamaKrishna[TetrahedronLetters,2017,vol.58,#29,p.2813-2817]

29334-16-5    1079-21-6   
4-((4-bromophenyl)(phenyl)methyl)-1,1’-biphenyl-2,5-diol 

[1]TetrahedronLetters,2017,vol.58,p.2813-2817

[1]InorganicaChimicaActa,2016,vol.444,p.159-165

Literature

Title: Phenylhydroquinone induces loss of thymocytes through cell cycle arrest and apoptosis elevation in p53-dependent pathway.

Journal: The Journal of toxicological sciences 20130101

Title: Discovery of novel SERCA inhibitors by virtual screening of a large compound library.

Journal: European journal of medicinal chemistry 20110501

Title: Effective melanoma immunotherapy in mice by the skin-depigmenting agent monobenzone and the adjuvants imiquimod and CpG.

Journal: PloS one 20100101

Title: Structure-based virtual screening for novel inhibitors of the sarco/endoplasmic reticulum calcium ATPase and their experimental evaluation.

Journal: Bioorganic & medicinal chemistry 20090201

Title: Induction of mitosis delay, apoptosis and aneuploidy in human cells by phenyl hydroquinone, an Ames test-negative carcinogen.

Journal: Genes & genetic systems 20090201

Title: Phenyl hydroquinone, an Ames test-negative carcinogen, induces Hog1-dependent stress response signaling.

Journal: The FEBS journal 20081101

Title: Microarray analysis of toxicogenomic effects of ortho-phenylphenol in Staphylococcus aureus.

Journal: BMC genomics 20080101

Title: Rat Urinary Bladder Carcinogenesis by Dual-Acting PPARalpha + gamma Agonists.

Journal: PPAR research 20080101

Title: Development of a new E. coli strain to detect oxidative mutation and its application to the fungicide o-phenylphenol and its metabolites.

Journal: Mutation research 20070402

Title: Ames test-negative carcinogen, ortho-phenyl phenol, binds tubulin and causes aneuploidy in budding yeast.

Journal: Mutation research 20070401

Title: Analysis of genotoxicity and the carcinogenic mode of action for ortho-phenylphenol.

Journal: Environmental and molecular mutagenesis 20050601

Title: Depigmenting action of phenylhydroquinone, an O-phenylphenol metabolite, on the skin of JY-4 black guinea-pigs.

Journal: Pigment cell research 20021201

Title: Orthophenylphenol and phenylhydroquinone residues in citrus fruit and processed citrus products after postharvest fungicidal treatments with sodium orthophenylphenate in California and Florida.

Journal: Journal of agricultural and food chemistry 20010501

Title: Oxidative damage to cellular and isolated DNA by metabolites of a fungicide ortho-phenylphenol.

Journal: Carcinogenesis 19990501

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:1079-21-6 Molecular Formula|1079-21-6 MDL|1079-21-6 SMILES|1079-21-6 [1,1'-Biphenyl]-2,5-diol |Organic_Building_Blocks