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2-Methyl-2-hexanamine, also known as tert-amylamine or trimethylpropylamine, is an organic compound with the chemical formula C6H15N. It is a colorless, flammable liquid with a strong, fishy odor. This amine is used as a solvent, a chemical intermediate, and a reagent in various industrial processes. It is also a component of some gasoline additives and can be found in trace amounts in some foods and beverages. Due to its potential health risks, including irritation to the eyes, skin, and respiratory system, as well as its classification as a hazardous substance, it is important to handle 2-methyl-2-hexanamine with caution and in accordance with safety regulations.

2626-64-4

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2626-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2626-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2626-64:
(6*2)+(5*6)+(4*2)+(3*6)+(2*6)+(1*4)=84
84 % 10 = 4
So 2626-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H17N/c1-4-5-6-7(2,3)8/h4-6,8H2,1-3H3

2626-64-4Relevant academic research and scientific papers

Palladium-Catalyzed Arylation of Unactivated γ-Methylene C(sp3)-H and δ-C-H Bonds with an Oxazoline-Carboxylate Auxiliary

Ling, Peng-Xiang,Fang, Sheng-Long,Yin, Xue-Song,Chen, Kai,Sun, Bo-Zheng,Shi, Bing-Feng

supporting information, p. 17503 - 17507 (2016/01/25)

A palladium-catalyzed arylation of unactivated γ-methylene C(sp3)-H and remote δ-C-H bonds by using an oxazoline-carboxylate directing group has been developed. Arylation occurs with a broad substrate scope and high tolerance of functional groups (i.e., halogen, nitro, cyano, ether, trifluoromethyl, amine, and ester). The oxazoline-type auxiliary can be removed under acidic conditions.

Thiadiaziridine 1,1-Dioxides: Synthesis and Chemistry

Timberlake, Jack W.,Alender, Jeff,Garner, Archie W.,Hodges, Melvin L.,Oezmeral, Cenan,et al.

, p. 2082 - 2089 (2007/10/02)

The synthesis and chemical reactions of a series of thiadiaziridine 1,1-dioxides (2) are described.The thermal stability is highly dependent on the R group and in one case (R = tert-octyl) is postulated that the thermolysis initially produces a diradical intermediate which can be trapped or further fragments to give a nitrene.A temperature-dependent NMR study on the coalescence of the diastereotopic α-methyl protons of 2b gives a ΔG = 20 kcal*mol-1.

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