Английская Википедия:2-Methylnaphthalene-1,4-diamine

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Версия от 13:52, 21 декабря 2023; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox | ImageFile = Vitamin K6.svg | PIN = 2-Methylnaphthalene-1,4-diamine |Section1={{Chembox Identifiers | CASNo = 83-68-1 | CASNo_Ref = {{cascite|correct|CAS}} | UNII_Ref = {{fdacite|correct|FDA}} | UNII = YL68XZ7ZVU | PubChem = 9837191 | ChemSpiderID = 8012912 | EC_number = | DTXSID = DTXSID30431565 | StdInChI = 1S/C11H12N2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,12-13H2,1H3...»)
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Шаблон:Chembox 2-Methylnaphthalene-1,4-diamine is a synthetic menadione analog with vitamin K activity.[1][2]

2-Methylnaphthalene-1,4-diamine was first synthesized in 1925.[3][1] In 1942 two different research groups noted the vitamin K activity of the compound.[1][4][5] It forms a dihydrochloride salt (C11H14Cl2N2) with hydrochloric acid and one of the aforementioned research groups suggested the name vitamin K6 for the salt.[1]

2-Methylnaphthalene-1,4-diamine and its dihydrochloride can be made from 2-methylnaphthalene or its close analogs. Dihydrochloride blackens without melting at about 300 °C.[1]

4-Amino-3-methyl-1-naphthol or its dihydrochloride have not been used as commercial medicinal forms of vitamin K unlike phylloquinone and menadione for example.[6]

Oral toxicity of dihydrochloride for rats is approximately the same as for 4-amino-2-methyl-1-naphthol hydrochloride.[1]

References

Шаблон:Reflist

Шаблон:Vitamin Шаблон:Antihemorrhagics

Шаблон:Amine-stub