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123-08-0

  • Product Name4-Hydroxybenzaldehyde
  • Molecular FormulaC7H6O2
  • Molecular Weight122.123
  • Purity99%
  • Appearanceyellow to light brown crystalline powder
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Product Details

Quick Details

  • CasNo： 123-08-0
  • Molecular Formula： C7H6O2
  • Appearance： yellow to light brown crystalline powder
  • Purity： 99%

Excellent chemical plant bulk supply 4-Hydroxybenzaldehyde 123-08-0

  • Molecular Formula:C7H6O2
  • Molecular Weight:122.123
  • Appearance/Colour:yellow to light brown crystalline powder 
  • Vapor Pressure:0.0171mmHg at 25°C 
  • Melting Point:112-116°C(lit.) 
  • Refractive Index:1.618 
  • Boiling Point:246.6 °C at 760 mmHg 
  • Flash Point:101.3 °C 
  • PSA：37.30000 
  • Density:1.226 g/cm3 
  • LogP:1.20470 

4-Hydroxybenzaldehyde(Cas 123-08-0) Usage

Chemical Description

4-hydroxybenzaldehyde is an organic compound with a hydroxyl group and an aldehyde group.

Chemical Composition and Structure

4-Hydroxybenzaldehyde (4-HBA) is an organic compound belonging to the class of hydroxybenzaldehydes. It is characterized by a benzene ring with a hydroxyl group (-OH) and an aldehyde group (-CHO) attached at the para position.

Sources

4-Hydroxybenzaldehyde is found naturally in plants such as Gastrodia elata (Tianma) and Vanilla planifolia (vanilla orchid). It can also be synthesized chemically.

Mechanism of Action

4-Hydroxybenzaldehyde has been studied for its various biological activities, including its ability to inhibit GABA transaminase, modulate bacterial metabolism, and act as a flavoring agent. Its mechanism of action involves interactions with specific molecular targets, such as enzymes and receptors.

InChI:InChI=1/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H

123-08-0 Relevant articles

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Brady,Jakobovits

, p. 767,769, 777 (1950)

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Specific Catalysis by α-Cyclodextrin on the Dichlorocarbene Attack at Phenolate

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, p. 2053 - 2056 (1981)

A selsctive attack of dichlorocarbene at...

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Amakasu,T.,Sato,K.

, p. 1428 - 1432 (1967)

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Kratzl,Billek

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Figueiredo, Paulo,Lima, Jo?o C.,Santos, Helena,Wigand, Marie-Claude,Brouillard, Raymond,Ma?anita, António L.,Pina, Fernando

, p. 1249 - 1254 (1994)

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Hodgson,Jenkinson

, p. 469,470 (1929)

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Herbert, Richard B.,Mann, Jonathan

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(2S)-Tyrosine (5) is incorporated stereo...

A highly stable zeotype mesoporous zirconium metal-organic framework with ultralarge pores

Feng, Dawei,Wang, Kecheng,Liu, Tian-Fu,Park, Jihye,Wei, Zhangwen,Bosch, Mathieu,Zhou, Hong-Cai,Su, Jie,Zou, Xiaodong,Yakovenko, Andrey

, p. 149 - 154 (2015)

Through topological rationalization, a z...

Copper and manganese: Two concordant partners in the catalytic oxidation of p-cresol to p-hydroxybenzaldehyde

Wang, Feng,Yang, Guan-Yu,Zhang, Wei,Wu, Wen-Hai,Xu, Jie

, p. 1172 - 1173 (2003)

Copper and manganese were found to be tw...

PHOTOCATALYTIC OXIDATION OF p-CRESOL IN AQUEOUS TITANUM DIOXIDE SUSPENSION

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, p. 1285 - 1293 (1993)

The reaction products of the photocataly...

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Tsuji,Ohno

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Kojima, Satoshi,Hirano, Takashi,Niwa, Haruki,Ohashi, Mamoru,Inouye, Satoshi,Tsuji, Frederick I.

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A model compound, 4-(4-hydroxypheny])met...

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Omura,Matsuura

, p. 1516 (1969)

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, p. 3555 - 3558 (2020)

This study establishes the applicability...

Acid-promoted reaction of the stilbene antioxidant resveratrol with nitrite ions: Mild phenolic oxidation at the 4′-hydroxystiryl sector triggering nitration, dimerization, and aldehyde-forming routes

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In 0.1 M phosphate buffer, pH 3.0, and a...

The Enzyme-catalysed Electrochemical Conversion of p-Cresol into p-Hydroxybenzaldehyde

Hill, H. Allen O.,Oliver, B. Nigel,Page, David J.,Hopper, David J.

, p. 1469 - 1471 (1985)

The electrochemical oxidation of p-creso...

Absolute structures of C-glucosides of resveratrol oligomers from Shorea uliginosa

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Two C-glucosides of resveratrol dimers (...

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123-08-0 Process route

4-(1,3-dithiolan-2-yl)phenol
22068-49-1

4-(1,3-dithiolan-2-yl)phenol

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

4-hydroxy-3-nitrobenzaldehyde
3011-34-5

4-hydroxy-3-nitrobenzaldehyde

4-hydroxy-benzaldehyde
123-08-0,65581-83-1

4-hydroxy-benzaldehyde

4-[1,3]dithiolan-2-yl-2-nitro-phenol

4-[1,3]dithiolan-2-yl-2-nitro-phenol

Conditions
Conditions Yield
With bismuth(III) nitrate; water; In benzene; at 20 ℃; for 8h; Product distribution;
methyl p-hydroxycinnamate
3943-97-3,19367-38-5,61240-27-5

methyl p-hydroxycinnamate

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

3‐nitro‐p‐coumaric acid methyl ester
90729-87-6

3‐nitro‐p‐coumaric acid methyl ester

C<sub>10</sub>H<sub>11</sub>ClO<sub>4</sub>

C10H11ClO4

4-hydroxy-benzaldehyde
123-08-0,65581-83-1

4-hydroxy-benzaldehyde

Conditions
Conditions Yield
With hydrogenchloride; water; dihydrogen peroxide; sodium hydroxide; sodium nitrite; In aq. buffer;

123-08-0 Upstream products

  • 50-00-0
    50-00-0

    formaldehyd

  • 139-02-6
    139-02-6

    sodium phenoxide

  • 64-18-6
    64-18-6

    formic acid

  • 27914-73-4
    27914-73-4

    4-acetoxybenzoyl chloride

123-08-0 Downstream products

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    27559-50-8

    (E)-3-(4-hydroxyphenyl)-N-phenylacrylamide

  • 500859-97-2
    500859-97-2

    4-hydroxy-3-(piperidin-1-ylmethyl)benzaldehyde

  • 486-30-6
    486-30-6

    2-(4-hydroxyphenyl)-2-(piperidin-1-yl)acetonitrile

  • 3421-18-9
    3421-18-9

    2,5-dimorpholinocyclohexa-2,5-diene-1,4-dione

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