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Merck

498289

Sigma-Aldrich

3-Ethynylaniline

≥98%

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About This Item

Fórmula lineal:
HC≡CC6H4NH2
Número de CAS:
Peso molecular:
117.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥98%

reaction suitability

reaction type: click chemistry

storage temp.

2-8°C

SMILES string

Nc1cccc(c1)C#C

InChI

1S/C8H7N/c1-2-7-4-3-5-8(9)6-7/h1,3-6H,9H2

InChI key

NNKQLUVBPJEUOR-UHFFFAOYSA-N

General description

3-Ethynylaniline is a terminal alkyne that can be prepared by the reduction of 3-ethylnylnitrobenzene.

Application

3-Ethynylaniline may be used in the synthesis of the following benzoxazine monomers:
  • bis{4-[3-(3-ethynylphenyl)(2H,4Hbenzo[3,4-e]1,3-oxazin-6-yloxy)]phenyl}phenylphosphino-1-one
  • [3-(3-ethynylphenyl)(2H,4Hbenzo[3,4-e]1,3-oxazaperhydroin-6-yl)][3-(3-ethynylphenyl)(2H,4H-benzo[3,4-e]1,3-oxazin-6-yl)]phenylphosphino-1-one
  • bis[3-(3-ethynylphenyl)(2H,4Hbenzo[3,4-e]1,3-oxazin-6-yl)oxy]phenylphosphino-1-one
It may be used:
  • To synthesize succin(m-ethynyl)dianilide and sebaco(m-ethynyl)dianilide.
  • As a reagent in the multi-step synthesis of erlotinib hydrochloride.
  • To prepare 3-(3-ethynylphenyl)-6-methyl-2H, 4H-benzo[e]1,3-oxazine.
  • To prepare 3-[3-(4-acetylamino-benzyl)-[1,2,4]oxadiazol-5- yl]-N-(3-ethynyl-phenyl)-propionamide.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Diacetylene-Containing Polymers III. Poly (m,m'-butadiynylenesuccindianilide) and Poly (m,m'-butadiynylene sebacodianilide): Novel Materials for Preparation of Transparent Polydiacetylene Containing Films.
Fomine S and Ogawa T
Polymer Journal, 26(1), 93-98 (1994)
Preparation of 2'-aminoacetophenones: a one-pot hydration and reduction of 1-ethynyl-2-nitrobenzenes.
Bosch E and Jeffries L.
Tetrahedron Letters, 42(46), 8141-8142 (2001)
Modified synthesis of erlotinib hydrochloride.
Barghi L, et al.
Advanced Pharmaceutical Bulletin, 2(1), 119-122 (2012)
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Large doses of chemical pesticides are required to achieve effective concentrations in the rhizosphere, which results in the accumulation of harmful residues. Precision farming is needed to improve the efficacy of pesticides, but also to avoid environmental pollution, and slow-release
Side-chain type benzoxazine-functional cellulose via click chemistry.
Agag T, et al.
Journal of Applied Polymer Science, 125(2), 1346-1351 (2012)

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