Pharmaceutical intermediates & materials

Home - Products - Pharmaceutical intermediates & materials

4-Tolylboronic acid

  • Product Name: 4-Tolylboronic acid
  • CasNo: 5720-05-8
  • Purity:
  • Appearance: white to light yellow crystal powder

Mobile/Wechat/WhatsApp: Chen Shihuai +86-13961989018  Yang Zhengquan +86-13921613169   Chen Yi +86-13962066393

Email:

Inquiry

CasNo: 5720-05-8

Molecular Formula: C7H9BO2

Appearance: white to light yellow crystal powder

Manufacturer supply high quality 4-Tolylboronic acid 5720-05-8 with ISO standards

  • Molecular Formula:C7H9BO2
  • Molecular Weight:135.958
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.976mmHg at 25°C 
  • Melting Point:256-263 °C(lit.) 
  • Refractive Index:1.505 
  • Boiling Point:275.2 °C at 760 mmHg 
  • PKA:8.84±0.10(Predicted) 
  • Flash Point:120.2 °C 
  • PSA:40.46000 
  • Density:1.1 g/cm3 
  • LogP:-0.32520 

4-Tolylboronic acid(Cas 5720-05-8) Usage

InChI:InChI=1/C9H13N/c1-8(10-2)9-6-4-3-5-7-9/h3-8,10H,1-2H3/t8-/m1/s1

5720-05-8 Relevant articles

Atropisomerism of the C-1-C′-1 axis of 2,2′,8,8′-unsubstituted 1,1′-binaphthyl derivatives

Chow,Wan

, p. 5042 - 5047 (2001)

The Suzuki coupling of optically active ...

Bipyridinium and Phenanthrolinium Dications for Metal-Free Hydrodefluorination: Distinctive Carbon-Based Reactivity

Burton, Katherine I.,Elser, Iris,Waked, Alexander E.,Wagener, Tobias,Andrews, Ryan J.,Glorius, Frank,Stephan, Douglas W.

supporting information, p. 11730 - 11737 (2021/07/16)

The development of novel Lewis acids der...

Preparation method of trans-ketone intermediate

-

Paragraph 0086-0090; 0092, (2021/06/06)

The invention discloses a preparation me...

Aryl boronic acid preparation method

-

Paragraph 0029-0030, (2020/01/25)

The invention belongs to the technical f...

Palladium-catalyzed B-diarylation of diethylaminoborane for the synthesis of diarylborinic acids

Igarashi, Takuya,Shimazumi, Ryoma,Tobisu, Mamoru

supporting information, p. 760 - 763 (2020/07/10)

The palladium-catalyzed synthesis of dia...

5720-05-8 Process route

2,3-dihydro-2-(4-methylphenyl)benzo[d][1,3,2]diazaborinin-4(1H)-one
32203-14-8

2,3-dihydro-2-(4-methylphenyl)benzo[d][1,3,2]diazaborinin-4(1H)-one

4-methylphenylboronic acid
5720-05-8

4-methylphenylboronic acid

anthranilic acid amide
28144-70-9,88-68-6

anthranilic acid amide

Conditions
Conditions Yield
In 1,4-dioxane; water; at 140 ℃; for 0.5h; Microwave irradiation; Sealed tube;
88%
78%
Triisopropyl borate
5419-55-6

Triisopropyl borate

para-bromotoluene
106-38-7

para-bromotoluene

4-methylphenylboronic acid
5720-05-8

4-methylphenylboronic acid

Conditions
Conditions Yield
para-bromotoluene; With iodine; magnesium; In tetrahydrofuran; at 70 ℃; for 1h;
Triisopropyl borate; In tetrahydrofuran; at 0 ℃; for 1h; Temperature; Concentration; Time;
91%
With magnesium; ethylene dibromide; In tetrahydrofuran; at 40 - 60 ℃; for 6h; Inert atmosphere;
58%
para-bromotoluene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 - -10 ℃;
Triisopropyl borate; In tetrahydrofuran; hexane; at -78 - 20 ℃;
52%
With hydrogenchloride; n-butyllithium; In tetrahydrofuran; hexane;
para-bromotoluene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.25h; Inert atmosphere;
Triisopropyl borate; In tetrahydrofuran; hexane; at 25 ℃; for 0.333333h; Inert atmosphere;

5720-05-8 Upstream products

  • 4250-45-7
    4250-45-7

    dichloro-p-tolyl-borane

  • 66117-64-4
    66117-64-4

    di(p-tolyl)borinic acid

  • 13195-76-1
    13195-76-1

    triisobutyl borate

  • 4294-57-9
    4294-57-9

    para-methylphenylmagnesium bromide

5720-05-8 Downstream products

  • 34258-31-6
    34258-31-6

    6-bromo-2-p-tolyl-2,3-dihydro-1H-benzo[1,3,2]diazaborinin-4-one

  • 32203-14-8
    32203-14-8

    2,3-dihydro-2-(4-methylphenyl)benzo[d][1,3,2]diazaborinin-4(1H)-one

  • 58113-12-5
    58113-12-5

    3-(4-methylphenyl)-4H-chromen-4-one

  • 152684-18-9
    152684-18-9

    3-methoxy-5-(4-methylphenyl)-2-nitropyridine

Leave Your Message

Relevant Products