萘茜(英语:Naphthazarin,或称为5,8-二羟基-1,4-萘醌,5,8-dihydroxy-1,4-naphthoquinone,IUPAC名:5,8-二羟基-1,4-萘二酮,5,8-dihydroxy-1,4-naphthalenedione)是一种天然有机化合物,分子式C10H6O4,属于一种基于1,4-萘醌二羟基萘醌[1][2],可溶于1,4-二𫫇烷,常温常压下为深红色针状晶体,熔点为 228−232 °C[3]

萘茜
IUPAC名
5,8-Dihydroxynaphthalene-1,4-dione
别名 Dihydroxynaphthoquinone
识别
CAS号 475-38-7  ☒N
PubChem 10141
ChemSpider 9735
SMILES
 
  • C1=CC(=C2C(=O)C=CC(=O)C2=C1O)O
InChI
 
  • 1/C10H6O4/c11-5-1-2-6(12)10-8(14)4-3-7(13)9(5)10/h1-4,11-12H
InChIKey RQNVIKXOOKXAJQ-UHFFFAOYAN
EINECS 207-495-4
ChEBI 28849
KEGG C01938
性质
化学式 C10H6O4
摩尔质量 190.15 g·mol−1
熔点 228-232 °C(269 K)
危险性
GHS危险性符号
《全球化学品统一分类和标签制度》(简称“GHS”)中有害物质的标签图案
GHS提示词 Warning
H-术语 H302, H312, H315, H319, H332, H335
P-术语 P261, P264, P270, P271, P280, P301+312, P302+352, P304+312, P304+340, P305+351+338, P312, P321, P322, P330
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献

编辑
  1. ^ Thomson R.H. Naturally Occurring Quinones. Academic Press, London (1971). Quoted by Khalafy and Bruce.
  2. ^ Thomson R.H. Naturally Occurring Quinones III. Chapman and Hall, London (1987). Quoted by Khalafy and Bruce.
  3. ^ J. Khalafy and J.M. Bruce (2002), Oxidative dehydrogenation of 1-tetralones: Synthesis of juglone, naphthazarin, and α-hydroxyanthraquinones. Journal of Sciences, Islamic Republic of Iran, volume 13 issue 2, pages 131-139.