
2144-08-3
- Product Name:2,3,4-Trihydroxybenzaldehyde
- Molecular Formula:C7H6O4
- Purity:99%
- Molecular Weight:154.122
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
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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)
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2144-08-3 Process route
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109103-74-4
2,3,4-Trihydroxy-benzaldehyd-p-tolylimin

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

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106-49-0,12221-03-3
p-toluidine
Conditions | Yield |
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With
methanol; sodium tetrahydroborate;
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Multi-step reaction with 2 steps
1: [bis(acetoxy)iodo]benzene
2: sodium tetrahydroborate; methanol
With
methanol; sodium tetrahydroborate; [bis(acetoxy)iodo]benzene;
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C14H11NO3

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

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106-49-0,12221-03-3
p-toluidine
Conditions | Yield |
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With
methanol; sodium tetrahydroborate;
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2144-08-3 Upstream products
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N,N'-diphenylformamidine
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2-hydroxyresorcinol
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Formanilid
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hydrogen cyanide
2144-08-3 Downstream products
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2-(3,4-dihydroxy-phenyl)-3,7,8-trihydroxy-chromenylium; chloride
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formic acid
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7,8-diacetoxy-3-phenylcoumarin
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N-(2,3,4-trihydroxy-benzylidene)-p-hydroxyaniline
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