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1-Propen-2-amine, N,N-dimethyl-, also known as 2-dimethylaminopropene or N,N-dimethylallylamine, is an organic compound with the chemical formula C5H11N. It is a colorless liquid with a pungent odor and is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. 1-Propen-2-amine, N,N-dimethyl- is highly reactive due to the presence of the amine group and the allyl group, making it a versatile building block in organic synthesis. It is also known for its potential use as a corrosion inhibitor and as a monomer in the production of polymers. However, due to its reactivity and potential health hazards, it requires careful handling and is typically stored under controlled conditions.

22499-75-8

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22499-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22499-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22499-75:
(7*2)+(6*2)+(5*4)+(4*9)+(3*9)+(2*7)+(1*5)=128
128 % 10 = 8
So 22499-75-8 is a valid CAS Registry Number.

22499-75-8Relevant academic research and scientific papers

Thermolysis, Photolysis, and Acid Catalysis of an α-(Dimethylamino)azoalkane. Amino Stabilization of a Carbon Radical Center

Engel, Paul S.,Wu, Wen-Xue

, p. 2720 - 2725 (2007/10/02)

The unsymmetrical azoalkane 2-(tert-butylazo)-2-(dimethylamino)propane (7) has been synthesized cleanly by nucleophilic displacement of chloride from the corresponding α-chloroazoalkane 5 with dimethylamine.Thermolysis of 7 in hydrocarbon solvents affords typical radical-derived products and exhibits activation parameters ΔH(excit.) = 26.6 +/- 0.4 kcal/mol and ΔS(excit.) = -6.6 +/- 1.1 eu.Since the thermolysis rate of 7 is 104 faster than that of 1,2-di-tert-butyldiazene, the large stabilization of α-amino radicals is supported.Unusual products were obtained in acetonitrile, suggesting reduction of the azo linkage by 2-(dimethylamino)-2-propyl radicals and cleavage of the resulting hydrazyl radicals.In protic solvents, 7 undergoes acid catalyzed decomposition via tert-butyldiazene as a postulated intermediate.

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