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ChemicalBook--->CAS DataBase List--->33311-29-4

33311-29-4

33311-29-4 Structure

33311-29-4 Structure
IdentificationBack Directory
[Name]

4-(2-METHOXYETHOXY)ANILINE
[CAS]

33311-29-4
[Synonyms]

AKOS BC-2489
AKOS BBB/095
ALINDA 102942
ASISCHEM C40525
CHEMBRDG-BB 4003841
4-(2-Methoxyethoxy)
p-Phenetidine, β-methoxy-
4-(2-METHOXYETHOXY)ANILINE
4-(2-methoxyethoxy)phenylamine
4-(2-Methoxyethoxy)-benzenaMine
Benzenamine, 4-(2-methoxyethoxy)-
4-(2-methoxyethoxy)aniline(SALTDATA: HCl)
4-(2-METHOXYETHOXY)ANILINE ISO 9001:2015 REACH
[Molecular Formula]

C9H13NO2
[MDL Number]

MFCD03004838
[MOL File]

33311-29-4.mol
[Molecular Weight]

167.21
Chemical PropertiesBack Directory
[Boiling point ]

142 °C(Press: 3 Torr)
[density ]

1.078±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

5.10±0.10(Predicted)
[Appearance]

Light brown to brown Solid
[InChI]

InChI=1S/C9H13NO2/c1-11-6-7-12-9-4-2-8(10)3-5-9/h2-5H,6-7,10H2,1H3
[InChIKey]

DIOBEQCFVVJJBU-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(OCCOC)C=C1
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2922290090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(2-METHOXYETHOXY)ANILINE(33311-29-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-NITROPHENYL-2-METHOXYETHYL ETHER

22483-40-5

4-(2-METHOXYETHOXY)ANILINE

33311-29-4

General procedure for the synthesis of 4-(2-methoxyethoxy)aniline from 4-nitrophenyl-2-methoxyethyl ether: 1-(2-methoxyethoxy)-4-nitrobenzene (38) (3.9 g, 20 mmol), methanol (80 mL), and 10% activated carbon (400 mg) were added to a hydrogenation reactor. The reaction mixture was stirred overnight at room temperature in a hydrogen atmosphere. Upon completion of the reaction, the mixture was filtered through diatomaceous earth to remove the activated carbon. The filtrate was concentrated in vacuum to afford 4-(2-methoxyethoxy)aniline (39) (3.1 g, 93% yield) as a black oily product. m/z (M+1) 168.1 was shown by LC-MS (ESI) analysis.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 21, p. 5177 - 5181
[2] Patent: CN103864792, 2017, B. Location in patent: Paragraph 0313; 0314; 0315; 0316
[3] Patent: WO2015/131080, 2015, A1. Location in patent: Paragraph 00768; 00770
[4] Patent: WO2014/130693, 2014, A1. Location in patent: Paragraph 00544; 00547
[5] European Journal of Medicinal Chemistry, 1980, vol. 15, # 5, p. 399 - 404
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