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336572

Sigma-Aldrich

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:
2835-97-4
Molecular Weight:
123.15
MDL number:
MFCD00075082
UNSPSC Code:
12352100
PubChem Substance ID:
24860396
NACRES:
NA.22

assay

96%

mp

149-152 °C (lit.)

SMILES string

Cc1cccc(O)c1N

InChI

1S/C7H9NO/c1-5-3-2-4-6(9)7(5)8/h2-4,9H,8H2,1H3

InChI key

FEDLEBCVFZMHBP-UHFFFAOYSA-N

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.[1]

Application

2-Amino-3-methylphenol was used in the preparation of Schiff base ligands.[2]

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD9919V
WXBD1399V
STBG9516
STBD7858V
06219HH

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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)
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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