2144-08-3

  • Product Name:2,3,4-Trihydroxybenzaldehyde
  • Molecular Formula:C7H6O4
  • Purity:99%
  • Molecular Weight:154.122
Inquiry

Product Details

pd_meltingpoint:159-161 °C(lit.)

Appearance:light brown to beige-brown powder

Factory Sells Best Quality 2,3,4-Trihydroxybenzaldehyde 2144-08-3 with USP

  • Molecular Formula:C7H6O4
  • Molecular Weight:154.122
  • Appearance/Colour:light brown to beige-brown powder 
  • Vapor Pressure:0.000573mmHg at 25°C 
  • Melting Point:159-161 °C(lit.) 
  • Refractive Index:1.734 
  • Boiling Point:301.9 °C at 760 mmHg 
  • PKA:7.41±0.23(Predicted) 
  • Flash Point:150.6 °C 
  • PSA:77.76000 
  • Density:1.598 g/cm3 
  • LogP:0.61590 

2,3,4-Trihydroxybenzaldehyde(Cas 2144-08-3) Usage

General Description

Antimicrobial activity of carbohydrazone derived from 2,3,4-trihydroxybenzaldehyde against bacteria and fungi has been investigated. 2,3,4-trihydroxybenzaldehyde forms Schiff bases via [1+1] condensation with anthranilic acid.

InChI:InChI=1/C7H6O4/c8-3-4-1-2-5(9)7(11)6(4)10/h1-3,9-11H

2144-08-3 Relevant articles

Synthesis method of 2,3,4-trihydroxyl benzaldehyde

-

Paragraph 0030-0034, (2021/05/26)

The invention provides a synthesis metho...

Dienaminodiones, new push-pull alkenes, from 3,4-dihydroxysalicylaldehyde-derived Schiff base

Ravindran, Jaice,Ingaladal, Nagaraja,Lankalapalli, Ravi S.

supporting information, (2020/10/20)

An atom-economical one-pot synthesis of ...

Benzyl and benzaldehyde-derived metabolites from desert actinomycetes Sp. CDS

Nazir, Mamona,Mustafa, Rizwana,Tousif, Muhammad Imran,Ahmad, Shabir,Khatoon, Tasneem,Ahmad, Ishtiaq

, p. 919 - 923 (2018/10/02)

Chromatographic purification of the cult...

Ubiquinones and related compounds. XXII. Synthesis of 2,3-dimethoxy-5-methyl-1,4-benzoquinone and its ethylhomologues

Sugihara,Watanabe,Kawamatsu,Morimoto

, p. 109 - 120 (2007/10/05)

-

2144-08-3 Process route

2,3,4-Trihydroxy-benzaldehyd-<i>p</i>-tolylimin
109103-74-4

2,3,4-Trihydroxy-benzaldehyd-p-tolylimin

2,3,4-trihydroxybenzylaldehyde
2144-08-3

2,3,4-trihydroxybenzylaldehyde

<i>p</i>-toluidine
106-49-0,12221-03-3

p-toluidine

Conditions
Conditions Yield
With methanol; sodium tetrahydroborate;
Multi-step reaction with 2 steps
1: [bis(acetoxy)iodo]benzene
2: sodium tetrahydroborate; methanol
With methanol; sodium tetrahydroborate; [bis(acetoxy)iodo]benzene;
C<sub>14</sub>H<sub>11</sub>NO<sub>3</sub>

C14H11NO3

2,3,4-trihydroxybenzylaldehyde
2144-08-3

2,3,4-trihydroxybenzylaldehyde

<i>p</i>-toluidine
106-49-0,12221-03-3

p-toluidine

Conditions
Conditions Yield
With methanol; sodium tetrahydroborate;

2144-08-3 Upstream products

  • 864131-95-3
    864131-95-3

    N,N'-diphenylformamidine

  • 87-66-1
    87-66-1

    2-hydroxyresorcinol

  • 103-70-8
    103-70-8

    Formanilid

  • 74-90-8
    74-90-8

    hydrogen cyanide

2144-08-3 Downstream products

  • 65618-22-6
    65618-22-6

    2-(3,4-dihydroxy-phenyl)-3,7,8-trihydroxy-chromenylium; chloride

  • 64-18-6
    64-18-6

    formic acid

  • 857783-33-6
    857783-33-6

    7,8-diacetoxy-3-phenylcoumarin

  • 100727-75-1
    100727-75-1

    N-(2,3,4-trihydroxy-benzylidene)-p-hydroxyaniline

Relevant Products