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183489-42-1

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183489-42-1 Usage

General Description

2,4-Pentadienenitrile,5-(dimethylamino)-(9CI) is a chemical compound that consists of a five-carbon chain with two carbon-carbon double bonds and a nitrile group. The presence of a dimethylamino group indicates that the compound also contains a nitrogen atom bonded to two methyl groups. 2,4-Pentadienenitrile,5-(dimethylamino)-(9CI) is commonly used as a building block in organic synthesis and can be used to create a variety of other chemical compounds. It has potential applications in the pharmaceutical and agrochemical industries, among others. Additionally, the dimethylamino group can influence the reactivity and properties of the compound, making it useful for a range of chemical reactions and processes. Overall, 2,4-Pentadienenitrile,5-(dimethylamino)-(9CI) 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).

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