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Merck
CN

168637

2,4-二羟基苯甲醛

98%

别名:

雷琐醛

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线性分子式:
(HO)2C6H3CHO
化学文摘社编号:
分子量:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-383-1
Beilstein/REAXYS Number:
878548
MDL number:
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产品名称

2,4-二羟基苯甲醛, 98%

InChI key

IUNJCFABHJZSKB-UHFFFAOYSA-N

InChI

1S/C7H6O3/c8-4-5-1-2-6(9)3-7(5)10/h1-4,9-10H

SMILES string

[H]C(=O)c1ccc(O)cc1O

assay

98%

form

powder

bp

220-228 °C/22 mmHg (lit.)

mp

135-137 °C (lit.)

functional group

aldehyde

Quality Level

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Application

2,4-二羟基苯甲醛用于两步法合成 3,5-二溴-2,4-二羟基肉桂酸乙酯

General description

2,4-二羟基苯甲醛可在极其温和的碱性条件下发生区域选择性单苄基化反应。它在甲醇中与异烟肼酸发生缩合反应,生成2,4-二羟基苯甲醛异烟酰腙,一种新的荧光试剂

2,4-二羟基苯甲醛是生物活性化合物、特种化学品和染料的潜在合成砌块。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Antibacterial activity and molecular studies of non-symmetric POCOP-Pd (II) pincer complexes derived from 2, 4-dihydroxybenzaldehyde (2, 4-DHBA)
Aragn-Muriel, A et al.
Polyhedron, 227, 116115-116115 (2022)
Two-photon uncaging with the efficient 3,5-dibromo-2,4-dihydroxycinnamic caging group.
Nathalie Gagey et al.
Angewandte Chemie (International ed. in English), 46(14), 2467-2469 (2007-02-21)
The regioselective 4-benzylation of 2, 4-dihydroxybenzaldehyde.
Mendelson WL, et al.
Synthetic Communications, 26(3), 593-601 (1996)
Direct and derivative spectrophotometric determination of zinc with 2, 4-dihydroxybenzaldehyde isonicotinoyl hydrazone in potable water and pharmaceutical samples.
Sivaramaiah S and Reddy PR.
Journal of Analytical Chemistry, 60(9), 828-832 (2005)
Fabien Vincent et al.
Bioorganic & medicinal chemistry letters, 19(23), 6793-6796 (2009-10-24)
The screening of known medicinal agents against new biological targets has been shown to be a valuable approach for revealing new pharmacology of marketed compounds. Recently, carbamate, urea and ketone inhibitors of fatty acid amide hydrolase (FAAH) have been described

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