2,5-diethoxyaniline

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Names

[ CAS No. ]:
94-85-9

[ Name ]:
2,5-diethoxyaniline

[Synonym ]:
MFCD00015144
2,5-Diethoxy aniline
Aminohydroquinone diethyl ether
Benzenamine,5-diethoxy
EINECS 202-369-5
2,5-Diaethoxy-anilin
2,5-Diethoxy-anilin
2,4-DIFLUORO-5-NITROBENZENESULFONYL CHLORIDE
Aniline,5-diethoxy
Benzenamine, 2,5-diethoxy-
2,5-diethoxyphenylamine
2,5-diethoxyaniline
Aniline, 2,5-diethoxy-
Aminohydrochinon-diaethylaether
1-amino-2,5-diethoxybenzene

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
304.0±22.0 °C at 760 mmHg

[ Melting Point ]:
85-88 °C(lit.)

[ Molecular Formula ]:
C10H15NO2

[ Molecular Weight ]:
181.232

[ Flash Point ]:
150.1±29.6 °C

[ Exact Mass ]:
181.110275

[ PSA ]:
44.48000

[ LogP ]:
2.10

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.527

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-S36

[ RIDADR ]:
2811

[ WGK Germany ]:
1

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2922299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Benzene,1,4-diethoxy-2-nitro-
  • Ethanol

DownStream

  • N-(2,5-Diethoxyphenyl)benzamide
  • Benzenamine,4,4'-(phenylmethylene)bis[2,5-diethoxy-

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

Reduction of aromatic nitro compounds to aromatic amines by sodium trimethylsilanethiolate. Hwu JR, et al.

J. Org. Chem. 57(19) , 5254-55, (1992)

Identification of Amines. II. Phthalimidomethyl Derivatives of Primary and Secondary Amines1. Heine HW, et al.

J. Am. Chem. Soc. 78(3) , 672-674, (1956)

Direct ring closure through the nitro group. Isomer formation in the synthesis of unsymmetrical phenazines, and some general observations on the phenazine syntheses. Vivian DL ,et al.

J. Org. Chem. 16(1) , 1-7, (1951)


More Articles

Related Compounds

  • N-Ethyl-2,5-diethoxyaniline
  • 4-nitro-2,5-diethoxyaniline
  • 4-chloro-2,5-diethoxyaniline
  • N,N-Diethyl-2,5-diethoxyaniline
  • 2,5-Diethoxyaniline hydrochloride
  • 4,4'-(phenylmethanediyl)bis(2,5-diethoxyaniline)
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 4-[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecyl)oxy]benzoic acid
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 2-((4-(3-chlorobenzyl)piperazin-1-yl)methyl)-1-methyl-1H-benzo[d]imidazole
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine