Home Other Building Blocks 643-58-3
643-58-3,MFCD00008517
Catalog No.:AA003HT8

643-58-3 | 2-Methylbiphenyl

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1g
98%
in stock  
$21.00   $15.00
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5g
98%
in stock  
$72.00   $50.00
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25g
98%
in stock  
$246.00   $172.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003HT8
Chemical Name:
2-Methylbiphenyl
CAS Number:
643-58-3
Molecular Formula:
C13H12
Molecular Weight:
168.2344
MDL Number:
MFCD00008517
SMILES:
Cc1ccccc1c1ccccc1
NSC Number:
5321
Properties
Properties
 
BP:
255.3°C at 760 mmHg  
Form:
Liquid  
MP:
°C  
Refractive Index:
n20/D 1.591(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
144  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Rotatable Bond Count:
1  
XLogP3:
3.9  

Downstream Synthesis Route

[1]CurrentPatentAssignee:CHANGZHOUUNIVERSITY-CN109180500,2019,ALocationinpatent:Paragraph0052-0055

[2]Xiang,Ming;Zhou,Chao;Yang,Xiu-Long;Chen,Bin;Tung,Chen-Ho;Wu,Li-Zhu[JournalofOrganicChemistry,2020,vol.85,#14,p.9080-9087]

[3]Ott;Smith[JournaloftheAmericanChemicalSociety,1955,vol.77,p.2325,2328]

[1]CurrentPatentAssignee:CHANGZHOUUNIVERSITY-CN109180500,2019,ALocationinpatent:Paragraph0042-0046;0061-0063;0068-0070

[2]Zhang,Lele;Cheng,Songbo;Hang;Defeng[AsianJournalofChemistry,2019,vol.31,#12,p.3009-3011]

[3]Boeckmann,Klaus;Voegtle,Fritz[ChemischeBerichte,1981,vol.114,#3,p.1048-1064]

[4]CurrentPatentAssignee:CHINESEACADEMYOFSCIENCES;CHINAPETROCHEMICALCORPORATION;InstituteofChemistry(in:CAS)-CN111116678,2020,ALocationinpatent:Paragraph0077;0120-0122;0128-0131

[5]CurrentPatentAssignee:JIANGSUYANGNONGCHEMICALCO.,LTD.-US2018/362450,2018,A1Locationinpatent:Paragraph0086;0087

[6]Campbell;Wang[JournaloftheChemicalSociety,1947,p.2186]

[7]Cooketal.[JournaloftheChemicalSociety,1950,p.139,146]

[8]Palopoli;Feil;Holtkamp;RichardsonJr.[JournalofMedicinalChemistry,1974,vol.17,#12,p.1333-1335]

[1]JournalofOrganicChemistry,1983,vol.48,p.963-969

[1]Meyers,A.I.;Himmelsbach,RichardJ.;Reuman,Michael[JournalofOrganicChemistry,1983,vol.48,#22,p.4053-4058]

[1]DokladyChemistry,1982,vol.266,p.356-359    Dokl.Akad.NaukSSSRSer.Khim.,1982,vol.266,p.874-878

Literature

Title: Palladium(0) deposited on PAMAM dendrimers as a catalyst for C-C cross coupling reactions.

Journal: Molecules (Basel, Switzerland) 20110110

Title: An efficient organocatalytic method for constructing biaryls through aromatic C-H activation.

Journal: Nature chemistry 20101201

Title: Replacement of imidazolyl by pyridyl in biphenylmethylenes results in selective CYP17 and dual CYP17/CYP11B1 inhibitors for the treatment of prostate cancer.

Journal: Journal of medicinal chemistry 20100812

Title: Isopropylidene substitution increases activity and selectivity of biphenylmethylene 4-pyridine type CYP17 inhibitors.

Journal: Journal of medicinal chemistry 20100708

Title: New Ras CAAX mimetics: design, synthesis, antiproliferative activity, and RAS prenylation inhibition.

Journal: Bioorganic & medicinal chemistry letters 20090915

Title: Inhibition of nucleoside transport by new analogues of 4-nitrobenzylthioinosine: replacement of the ribose moiety by substituted benzyl groups.

Journal: Journal of medicinal chemistry 20041021

Title: Analysis of electron transfer in substituted biphenylmethane.

Journal: Annals of the New York Academy of Sciences 20031201

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SDS
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