592609
4-Ethynyl-N,N-dimethylaniline
97%
Synonym(s):
1-Ethynyl-4-dimethylaniline, 4-Dimethylaminophenylacetylene
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CH≡CC6H4N(CH3)2
CAS Number:
Molecular Weight:
145.20
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
mp
49-53 °C (lit.)
functional group
amine
SMILES string
CN(C)c1ccc(cc1)C#C
InChI
1S/C10H11N/c1-4-9-5-7-10(8-6-9)11(2)3/h1,5-8H,2-3H3
InChI key
ZWMAYLMVFSCMMS-UHFFFAOYSA-N
General description
4-Ethynyl-N,N-dimethylaniline can be prepared via hydrolysis of 4-(3-methyl-3-hydroxy-1-butynyl)-N,N-dimethylaniline using potassium hydroxide in toluene.
Application
4-Ethynyl-N,N-dimethylaniline may be used to synthesize the following:
- copper(I) arylacetylide via reaction with copper(II)acetate
- N,N-dimethyl-4-(3-pyridinylethynyl)aniline via Sonogashira–Hagihara coupling with 3-iodopyridine
- [[5,15-bis[(40-dimethylamino)phenyl]ethynyl]-10,20-bis[(triisopropylsilyl)ethynyl]porphyrinato]magnesium(II) via reaction with dibromo magnesium porphyrin
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
"Soluble porphyrin donors for small molecule bulk heterojunction solar cells"
Hatano J, et al.
Journal of Materials Chemistry, 22(36), 19258-19263 (2012)
Beletskaya P.I, et al.
Tetrahedron Letters, 44(27), 5011-5013 (2003)
"Synthesis and crystal structures of phenylethynylpyridinium derivatives for second-order nonlinear optics"
Umezawa H, et al.
Bulletin of the Chemical Society of Japan, 78(02), 344-348 (2005)
?Donor-substituted 1,1,4,4-tetracyanobutadienes (TCBDs): new chromophores with efficient intramolecular charge-transfer interactions by atom-economic synthesis?
Michinobu T, et al.
Chemistry?A European Journal , 12(07), 1889-1905 (2006)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service