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A88204

Sigma-Aldrich

m-Anisidine

97%

Synonym(s):

3-Aminoanisole, 3-Methoxyaniline

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About This Item

Linear Formula:
CH3OC6H4NH2
CAS Number:
536-90-3
Molecular Weight:
123.15
Beilstein:
386119
EC Number:
208-651-4
MDL number:
MFCD00007783
UNSPSC Code:
12352100
PubChem Substance ID:
24891371
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.581 (lit.)

bp

251 °C (lit.)

mp

−1-1 °C (lit.)

density

1.096 g/mL at 25 °C (lit.)

SMILES string

COc1cccc(N)c1

InChI

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

InChI key

NCBZRJODKRCREW-UHFFFAOYSA-N

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Application

m-Anisidine is used in:
  • The synthesis of N-substituted-3-chloro-2-azetidinones, which are potential anthelmintic agents.
  • Rhodium-catalyzed synthesis of indoles and copper-catalyzed synthesis of benzimidazoles.
  • In the preparation of azocalix[4]arene dyes.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

258.8 °F - closed cup

Flash Point(C)

126 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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N-Substituted-3-chloro-2-azetidinones: synthesis and characterization of novel anthelmintic agents.
Kumar M V, et al.
Research Journal of Pharmaceutical, Biological and Chemical Sciences, 1(2), 52-58 (2010)
Indole synthesis via rhodium catalyzed oxidative coupling of acetanilides and internal alkynes.
Stuart D R, et al.
Journal of the American Chemical Society, 130(49), 16474-16475 (2008)
C? H Functionalization/C? N Bond Formation: Copper?Catalyzed Synthesis of Benzimidazoles from Amidines.
Brasche G and Buchwald S L
Angewandte Chemie (International Edition in English), 47(10), 1932-1934 (2008)
Yasemin Bektas et al.
Scientific reports, 6, 29554-29554 (2016-07-15)
Synthetic elicitors are drug-like compounds that are structurally distinct from natural defense elicitors. They can protect plants from diseases by activating host immune responses and can serve as tools for the dissection of the plant immune system as well as
Azocalixarenes. 1: synthesis, characterization and investigation of the absorption spectra of substituted azocalix [4] arenes.
Karc? F, et al.
Dyes and Pigments, 59(1), 53-61 (2003)
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