768-35-4

  • Product Name3-Fluorophenylboric Acid
  • MFC6H6BFO2
  • Molecular Weight139.922
  • Purity99%
  • Appearancewhite to light yellow crystal powder
Inquiry

Product Details

Quick Details

  • CasNo: 768-35-4
  • MF: C6H6BFO2
  • Appearance: white to light yellow crystal powder
  • Purity: 99%

Quality Manufacturer Supply 3-Fluorophenylboric Acid 768-35-4 Efficient Transportation Efficient Delivery

  • Molecular Formula:C6H6BFO2
  • Molecular Weight:139.922
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:2.01E-09mmHg at 25°C 
  • Melting Point:214-218 °C(lit.) 
  • Boiling Point:271.4 °C at 760 mmHg 
  • PKA:7.50±0.10(Predicted) 
  • Flash Point:117.9 °C 
  • PSA:40.46000 
  • Density:1.24 g/cm3 
  • LogP:-0.49450 

3-Fluorophenylboronic acid(Cas 768-35-4) Usage

Chemical Properties

white to light yellow crystal powder

Uses

suzuki reaction

Flammability and Explosibility

Notclassified

InChI:InChI=1/C26H4F20P2/c27-3-7(31)15(39)23(16(40)8(3)32)47(24-17(41)9(33)4(28)10(34)18(24)42)1-2-48(25-19(43)11(35)5(29)12(36)20(25)44)26-21(45)13(37)6(30)14(38)22(26)46/h1-2H2

768-35-4 Relevant articles

Chirality-Driven Mode of Binding of α-Aminophosphonic Acid-Based Allosteric Inhibitors of the Human Farnesyl Pyrophosphate Synthase (hFPPS)

Feng, Yuting,Park, Jaeok,Li, Shi-Guang,Boutin, Rebecca,Viereck, Peter,Schilling, Matthew A.,Berghuis, Albert M.,Tsantrizos, Youla S.

, p. 9691 - 9702 (2019/11/03)

Thienopyrimidine-based allosteric inhibi...

Copper-Catalyzed Monoorganylation of Trialkyl Borates with Functionalized Organozinc Pivalates

Fu, Ying,Gou, Bei-Lei,Shi, Chun-Zhao,Du, Zhengyin,Shen, Tong

, p. 4253 - 4257 (2018/09/18)

Organozinc pivalates, a recently develop...

Synthesis and evaluation of sulfonamide derivatives as potent Human Uric Acid Transporter 1 (hURAT1) inhibitors

Yang, Xintuo,Pang, Xuehai,Fan, Lei,Li, Xinghai,Chen, Yuanwei

supporting information, p. 1919 - 1922 (2017/04/10)

This letter presents synthesis and struc...

Development of a Concise Multikilogram Synthesis of LPA-1 Antagonist BMS-986020 via a Tandem Borylation-Suzuki Procedure

Smith, Michael J.,Lawler, Michael J.,Kopp, Nathaniel,McLeod, Douglas D.,Davulcu, Akin H.,Lin, Dong,Katipally, Kishta,Sfouggatakis, Chris

, p. 1859 - 1863 (2017/11/24)

The process development for the synthesi...

768-35-4 Process route

3-fluorobromobenzene
1073-06-9

3-fluorobromobenzene

3-fluorophenylboronic acid
768-35-4

3-fluorophenylboronic acid

Conditions
Conditions Yield
3-fluorobromobenzene; With diisobutylaluminium hydride; magnesium; lithium chloride; In tetrahydrofuran; toluene; at 20 ℃; for 15h; Inert atmosphere;
With Trimethyl borate; In tetrahydrofuran; toluene; at 0 ℃; Inert atmosphere;
With hydrogenchloride; water; In tetrahydrofuran; toluene; at 0 ℃; Inert atmosphere;
83%
3-fluorobromobenzene; With n-butyllithium; In tetrahydrofuran; toluene; at -78 ℃; for 1.5h; Inert atmosphere;
With Trimethyl borate; In tetrahydrofuran; toluene; at -78 - 20 ℃; for 1h; Inert atmosphere;
70%
3-fluorobromobenzene; With magnesium; In diethyl ether;
With Trimethyl borate; In diethyl ether; at 3 ℃; for 3h;
With hydrogenchloride; In diethyl ether;
3-fluorobromobenzene; With magnesium; In tetrahydrofuran;
With Trimethyl borate;
With hydrogenchloride; Further stages.;
3-fluorobromobenzene; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 3h;
With Trimethyl borate; In tetrahydrofuran; at -78 - 20 ℃;
With hydrogenchloride; In tetrahydrofuran; water; for 1h;
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere; Schlenk technique
1.2: -78 - 20 °C / Inert atmosphere; Schlenk technique
2.1: hydrogenchloride / water / 20 °C / Inert atmosphere; Schlenk technique
With hydrogenchloride; n-butyllithium; In tetrahydrofuran; water;
Trimethyl borate
121-43-7,63156-11-6

Trimethyl borate

3-fluorobromobenzene
1073-06-9

3-fluorobromobenzene

3-fluorophenylboronic acid
768-35-4

3-fluorophenylboronic acid

Conditions
Conditions Yield
With n-butyllithium; In tetrahydrofuran; N2; BuLi dropping into org. compd. soln. at -78°C, mixt. keeping 3 h, B-compd. soln. addn. dropwise at -78°C, mixt. allowing to warm to room temp. overnight , stirring 1 h with 10% HCl, extn. (Et2O); org. extracts washing (water), drying, solvent vac. removal;
With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 1h; Inert atmosphere;

768-35-4 Upstream products

  • 688-74-4
    688-74-4

    boric acid tributyl ester

  • 1073-06-9
    1073-06-9

    3-fluorobromobenzene

  • 625-98-9
    625-98-9

    3-chlorofluorobenzene

  • 121-43-7
    121-43-7

    Trimethyl borate

768-35-4 Downstream products

  • 448-53-3
    448-53-3

    tris(3-fluoro phenyl)boroxine

  • 152608-85-0
    152608-85-0

    1-(benzyloxy)-4-ethyl-2-(3-fluorophenyl)-5-<(6-methyl-6-cyanoheptyl)oxy>benzene

  • 1841-58-3
    1841-58-3

    3′-fluoro-(1,1′-biphenyl)-4-carboxylic acid

  • 402-67-5
    402-67-5

    3-fluoro-1-nitrobenzene

Relevant Products