336572
2-Amino-3-methylphenol
96%
Synonym(s):
2-Amino-m-cresol
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About This Item
Linear Formula:
H2NC6H3(CH3)OH
CAS Number:
Molecular Weight:
123.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
InChI
1S/C7H9NO/c1-5-3-2-4-6(9)7(5)8/h2-4,9H,8H2,1H3
SMILES string
Cc1cccc(O)c1N
InChI key
FEDLEBCVFZMHBP-UHFFFAOYSA-N
assay
96%
mp
149-152 °C (lit.)
General description
2-Amino-3-methylphenol is an aminophenol formed by incubating isopropyl-β-D-thiogalactopyranoside-induced E. coli JS996 strain cells with various nitroaromatic compounds.
Application
2-Amino-3-methylphenol was used in the preparation of Schiff base ligands.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and reactivity of novel cyclometallated complexes derived from [C, N, O] terdentate ligands. Crystal structure of [Pd {2, 3, 4-(MeO) 3 C 6 HC (H)[double bond, length half m-dash] N [2-(O) C 6 H 4]}(PPh 3)].
Fernandez A, et al.
New. J. Chem., 26(4), 398-404 (2002)
Construction of Escherichia coli strains for conversion of nitroacetophenones to ortho-aminophenols.
Venkateswarlu Kadiyala et al.
Applied and environmental microbiology, 69(11), 6520-6526 (2003-11-07)
The predominant bacterial pathway for nitrobenzene (NB) degradation uses an NB nitroreductase and hydroxylaminobenzene (HAB) mutase to form the ring-fission substrate ortho-aminophenol. We tested the hypothesis that constructed strains might accumulate the aminophenols from nitroacetophenones and other nitroaromatic compounds. We
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