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Merck
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文件

340618

Sigma-Aldrich

2,3-二氨基苯酚

97%

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About This Item

线性分子式:
(H2N)2C6H3OH
CAS号:
59649-56-8
分子量:
124.14
MDL號碼:
MFCD00075199
分類程式碼代碼:
12352100
PubChem物質ID:
24860835
NACRES:
NA.22

化驗

97%

mp

161-165 °C (lit.)

SMILES 字串

Nc1cccc(O)c1N

InChI

1S/C6H8N2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H,7-8H2

InChI 密鑰

PCAXITAPTVOLGL-UHFFFAOYSA-N

相关类别

一般說明

2,3-Diaminophenol is an aromatic diamine and forms Pd(II) and Pt(II) complexes. 2,3-Diaminophenol reacts with 2,4-pentanedione to yield the corresponding benzo[b][1,4]diazepinium salts. 2,3-Diaminophenol reacts with salicylaldehyde or 5-bromosalicylaldehyde in absolute ethanol to yield new unsymmetrical Schiff base.

應用

2,3-Diaminophenol was used:
  • in one-pot microwave assisted synthesis of amino-1,5-benzoxazepines and hydroxyl-1,5-benzodiazepines
  • in the electrosynthesis of poly(2,3-diaminophenol) via electro-oxidation
  • in a synthesis of tetradentate Schiff base complexes via reaction with salicylaldehyde or 5-bromosalicylaldehyde and metals such as Mn(III), Ni(II) and Cu(II)

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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4-氨基间苯二酚 盐酸盐 96%

Sigma-Aldrich

163171

4-氨基间苯二酚 盐酸盐

2,6-二氨基吡啶 98%

Sigma-Aldrich

D24404

2,6-二氨基吡啶

Constantinos G Neochoritis et al.
Journal of medicinal chemistry, 53(23), 8409-8420 (2010-11-06)
Amino-1,5-benzoxazepines 2 and 5 and hydroxyl-1,5-benzodiazepines 3 and 6 have been synthesized in one-pot solvent-free conditions from 2,3-diaminophenol and ketones through microwave assisted acid catalysis, the benzoxazepine/benzodiazepine ratio depending on the R(1) and R(3) aryl substituents. The otherwise inaccessible and
Unsymmetrical tetradentate Schiff base complexes derived from 2, 3-diaminophenol and salicylaldehyde or 5-bromosalicylaldehyde.
Ourari A, et al.
Transition Metal Chemistry, 31(2), 169-175 (2006)
Transition Met. Chem. (London), 31, 169-169 (2006)
M Pérez-Cabré et al.
Journal of inorganic biochemistry, 98(3), 510-521 (2004-02-28)
Pd(II) and Pt(II) new complexes with simple aromatic diamines were synthesised and characterised with the aim of studying their possible antitumour activity. The aromatic diamines chosen were 2,3-diaminotoluene (2,3 dat), 3,4-diaminotoluene (3,4 dat), 4,5-diaminoxylene (4,5 dax) and 2,3-diaminophenol (2,3 dap).
Electropolymerization of 2, 3-diaminophenol.
Del Valle MA, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 38(9), 1698-1703 (2000)
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