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Home > Encyclopedia > 3,4-Dimethoxyphenylboronic acid

3,4-Dimethoxyphenylboronic acid

3,4-Dimethoxyphenylboronic acid structure

3,4-Dimethoxyphenylboronic acid 

structure
  • CAS No:

    122775-35-3

  • Formula:

    C8H11BO4

  • Chemical Name:

    3,4-Dimethoxyphenylboronic acid

  • Synonyms:

    Boronic acid,B-(3,4-dimethoxyphenyl)-;Boronic acid,(3,4-dimethoxyphenyl)-;B-(3,4-Dimethoxyphenyl)boronic acid;3,4-Dimethoxyphenylboronic acid;3,4-Dimethoxybenzeneboronic acid

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

Description

white to light beige powder and granules

3,4-Dimethoxyphenylboronic acid Basic Attributes

181.98

181.98

DTXSID00370452

29319090

Characteristics

58.9

1.19±0.1 g/cm3(Predicted)

245-250 °C(lit.)

336.7±52.0 °C(Predicted)

157.4±30.7 °C

1.518

25 g/L

Safety Information

IRRITANT

NONH for all modes of transport

3

R36/37/38

37/39-26-36/37

Xi

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 96 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3,4-Dimethoxyphenylboronic acid Use and Manufacturing

Methods of Manufacturing

General procedure: To a solution of arylamine (0.5 mmol, 1.0 equiv) in MeOH(1.0 mL) was added HCl (0.5 mL, 1.5 mmol, 3.0 equiv), followed by H2O (0.5 ml). This mixture was stirred 2 min, and the NaNO2 solution (0.25 mL) was then added. The NaNO2 solution was prepared by dissolving 35 mg ofNaNO2 in H2O (0.25 mL). This mixture was stirred 30 minat 0–5 °C, followed by HCl (135 mg, 1.5 mmol, 3.0 equivalents) in MeOH (1.0 mL). This mixture was stirred 60min. H2O (10 mL) was added to reaction mixture, then extracted with CH2Cl2 (50 mL, 3×). The combined organic layer was dried over Na2SO4, followed by evaporation to give the products.

Uses

suzuki reaction

Computed Properties

Molecular Weight:181.98
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:182.0750390
Monoisotopic Mass:182.0750390
Topological Polar Surface Area:58.9
Heavy Atom Count:13
Complexity:153
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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