製品名:(S)-2-(1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethan-1-amine (S)-2-(4-isobutylphenyl)propanoate

IUPAC Name:(2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid; 2-[(8S)-1H,2H,6H,7H,8H-indeno[5,4-b]furan-8-yl]ethan-1-amine

CAS番号:1227056-68-9
分子式:C26H35NO3
純度:98%
カタログ番号:CM555638
分子量:409.57

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CM555638-250mg in stock ƴijǎ
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製品詳細

CAS番号:1227056-68-9
分子式:C26H35NO3
融点:-
SMILESコード:OC([C@H](C1=CC=C(CC(C)C)C=C1)C)=O.NCC[C@@H]2CCC3=CC=C4OCCC4=C23
密度:
カタログ番号:CM555638
分子量:409.57
沸点:
MDL番号:
保管方法:Store at room temperature

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.
Benzofurans
Benzofuran is an aromatic heterocyclic organic compound with the chemical formula C8H6O. It is a colorless oily liquid at room temperature with an aromatic odor. Benzofuran can be volatilized with water vapor and can be decomposed by potassium permanganate and other oxidants. It is an intermediate for the preparation of amiodarone and indene resin. Benzofuran derivatives are important pharmaceutical intermediates.
Benzofuran | C8H6O | CID 9223 -Chemenu
Benzofuran | C8H6O | CID 9223 |Where to Buy Benzofurans
Benzofuran is the heterocyclic compound consisting of fused benzene and furan rings. This colourless liquid is a component of coal tar.Benzofuran is extracted from coal tar. It is also obtained by dehydrogenation of 2-ethylphenol.