183489-42-1 Usage
Molecular Structure
A five-carbon chain with two carbon-carbon double bonds and a nitrile group.
Functional Groups
Nitrile, dimethylamino.
Carbon-Carbon Double Bonds
Two double bonds in the molecule contribute to its reactivity and properties.
Nitrogen Atom
The presence of a nitrogen atom bonded to two methyl groups indicates the presence of a dimethylamino group.
Building Block
Commonly used as a building block in organic synthesis to create a variety of other chemical compounds.
Applications
Potential applications in the pharmaceutical and agrochemical industries, among others.
Reactivity
The dimethylamino group can influence the reactivity of the compound, making it useful for a range of chemical reactions and processes.
Diversity
Has diverse potential applications in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 183489-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,4,8 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 183489-42:
(8*1)+(7*8)+(6*3)+(5*4)+(4*8)+(3*9)+(2*4)+(1*2)=171
171 % 10 = 1
So 183489-42-1 is a valid CAS Registry Number.
183489-42-1Relevant articles and documents
Aminodienylesters. I: The cycloaddition reactions of tert- aminodienylester with α,β-unsaturated carbonyl compounds, styrenes, and quinones
Koike, Takeshi,Tanabe, Mituharu,Takeuchi, Naoki,Tobinaga, Seisho
, p. 243 - 248 (2007/10/03)
Methyl 5-(N,N-dimethylamino)-2,4-pentadienoate (tert-aminodienylester 1) was synthesized by condensation of methyl crotonate (2) with N,N,N',N'- tetramethylenediamine (3). The reactivity of 1 was investigated with methyl propiolate (4), dimethyl 2-butynedionate (5), dimethyl maleate (6), dimethyl fumarate (7), 2-buten-4-olide (8), 2-cyclohexenone (9), styrene (10), trans- β-nitrostyrene (11), 1,4-benzoquinone (19), methyl 1,4-naphthoquinone-5- carboxylate (21), 1,4-naphthoquinone (24), juglone (26), 5-methoxy-1,4- naphthoquinone (28), naphthazarin (31), and naphthazarin dimethyl ether (33). In addition, 5-(N,N-dimethylamino)-2,4-pentadienenitrile (tert-aminodienyl- nitrile 37) was synthesized by condensation of crotononitrile (36) with 3. The reactivity of 37 was investigated with dimethyl 2-butynedionate (5), and 2-cyclohexenone (9).
