Name: Name:3-Biphenylboronic acid
Brand: AABLOCKS
SKU: AA0034G1
Rating: 90 (10 reviews)

Catalog No.: AA0034G1

5122-95-2 | 3-Biphenylboronic acid

Pack Size： 250mg

Purity： 98%

in stock

$9.00 $6.00

Pack Size： 1g

Purity： 98%

in stock

$10.00 $7.00

Pack Size： 5g

Purity： 98%

in stock

$13.00 $9.00

Pack Size： 10g

Purity： 98%

in stock

$16.00 $11.00

Pack Size： 25g

Purity： 98%

in stock

$29.00 $20.00

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Technical Information

Catalog Number: AA0034G1

Chemical Name: 3-Biphenylboronic acid

CAS Number: 5122-95-2

Molecular Formula: C12H11BO2

Molecular Weight: 198.0255

MDL Number: MFCD28978177

SMILES: OB(c1cccc(c1)c1ccccc1)O

Properties

BP: 411°C at 760 mmHg

Form: Solid

MP: 193-198 °C(lit.)

Storage: Keep in dry area;2-8℃;

Complexity: 190

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 15

Hydrogen Bond Acceptor Count: 2

Hydrogen Bond Donor Count: 2

Isotope Atom Count: 0

Rotatable Bond Count: 2

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

Upstream Synthesis Route

2113-57-7

5122-95-2

[1]Patent:WO2010/5066,2010,A1,.Locationinpatent:Page/Pagecolumn178-179

[2]BioorganicandMedicinalChemistryLetters,2003,vol.13,#21,p.3813-3816

[3]AngewandteChemie-InternationalEdition,2008,vol.47,#6,p.1115-1118

121-43-7

2113-57-7

5122-95-2

[1]JournalofPhysicalChemistryB,2001,vol.105,#37,p.8845-8860

[2]JournalofPhysicalChemistryB,2001,vol.105,#37,p.8845-8860

[3]Patent:WO2013/12298,2013,A1,.Locationinpatent:Paragraph129-130

[4]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1995,#13,p.1733-1738

[5]Patent:US5914327,1999,A,

5419-55-6

2113-57-7

5122-95-2

[1]Patent:US2007/167654,2007,A1,.Locationinpatent:Page/Pagecolumn19

[2]Patent:US2002/19527,2002,A1,

688-74-4

103068-18-4

5122-95-2

[1]JournaloftheAmericanChemicalSociety,1934,vol.56,p.1850,1856

108-36-1

5122-95-2

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#21,p.3813-3816

[2]Patent:WO2013/12298,2013,A1,

Downstream Synthesis Route

10557-85-4

5122-95-2

4-(3-biphenyl)-3,5-dimethylisoxazole

[1]SyntheticCommunications,1994,vol.24,p.709-719

5122-95-2

90914-41-3

108-42-9

(3-biphenyl-3-yl-1<i>H</i>-pyrazolo3,4-<i>d</i>pyrimidin-4-yl)-(3-chloro-phenyl)-amine

[1]OrganicLetters,2003,vol.5,p.3587-3590

151583-29-8

5122-95-2

911497-15-9

[1]JournalofMedicinalChemistry,2006,vol.49,p.5804-5814

959912-60-8

5122-95-2

3-(biphenyl-3-yl)-5,5-dimethyl-2-(morpholin-4-yl)-5,6-dihydro-1-benzothiophen-7(4H)-one

[1]Patent:WO2007/141504,2007,A1.Locationinpatent:Page/Pagecolumn87

2113-57-7

5122-95-2

[1]Patent:WO2010/5066,2010,A1.Locationinpatent:Page/Pagecolumn178-179

[2]BioorganicandMedicinalChemistryLetters,2003,vol.13,p.3813-3816

[3]AngewandteChemie-InternationalEdition,2008,vol.47,p.1115-1118

Literature fold

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

Journal: Journal of medicinal chemistry20081127

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