2-Amino-3-methylphenol

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Names

[ CAS No. ]:
2835-97-4

[ Name ]:
2-Amino-3-methylphenol

[Synonym ]:
2-Hydroxy-6-methylanilin
Phenol,2-amino-3-methyl
amino-3-methylphenol
2-amino-m-cresol
2-Amino-3-methylphenol
Phenol, 2-amino-3-methyl-
2,6'-DIMETHOXY-2'-HYDROXYCHALCONE 0.993
EINECS 2835-97-4
2-hydroxy-6-methylaniline
2-azanyl-3-methyl-phenol
2-amino 3-methyl phenol
3-methyl-2-aminophenol
MFCD00075082

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
240.0±28.0 °C at 760 mmHg

[ Melting Point ]:
149-152 °C(lit.)

[ Molecular Formula ]:
C7H9NO

[ Molecular Weight ]:
123.152

[ Flash Point ]:
98.9±24.0 °C

[ Exact Mass ]:
123.068413

[ PSA ]:
46.25000

[ LogP ]:
0.90

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.616

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • WNR BQ F1
  • O-(3-methylphenyl)hydroxylamine
  • m-Cresol
  • 2-Methylphenyl azide
  • Ammonia

DownStream

  • WNR BQ F1
  • ethyl 5-methyl-3,4-dihydro-2h-1,4-benzoxazine-2-carboxylate
  • 1H-Indazol-7-ol
  • 2-Chloro-4-methyl-1,3-benzoxazole
  • 7-Methoxyindazole
  • 5-Methyl-2H-1,4-benzoxazin-3(4H)-one
  • 2,6-dichloro-m-cresol
  • 2,4-dichloro-m-cresol
  • 5-methyl-6-nitro-4H-1,4-benzoxazin-3-one
  • 2-Bromo-3-methylphenol

Customs

[ HS Code ]: 2922299090

[ Summary ]:
2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Construction of Escherichia coli strains for conversion of nitroacetophenones to ortho-aminophenols.

Appl. Environ. Microbiol. 69(11) , 6520-6, (2003)

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 ...

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)]. Fernández A, et al.

New J. Chem. 26(4) , 398-404, (2002)


More Articles

Related Compounds

  • 2-Amino-3-chloro-5-methylphenol
  • 2-Amino-5-bromo-3-methylphenol
  • 2-Amino-4-bromo-3-methylphenol
  • 2-AMINO-3-BENZYL-5-(4-METHOXYPHENYL)PYRAZINE
  • 2-amino-3-(naphthalen-1-ylmethylamino)but-2-enedinitrile
  • 2-amino-3-(indol-3-ylidenemethylamino)but-2-enedinitrile