推荐产品
质量水平
方案
98%
沸点
333-335 °C (lit.)
mp
65-67 °C (lit.)
溶解性
water: soluble 2000 part(lit.)
acetone: soluble(lit.)
alcohol: soluble(lit.)
chloroform: soluble(lit.)
diethyl ether: soluble(lit.)
petroleum ether: slightly soluble(lit.)
vegetable oils: soluble(lit.)
SMILES字符串
CCCCCCc1ccc(O)cc1O
InChI
1S/C12H18O2/c1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h7-9,13-14H,2-6H2,1H3
InChI key
WFJIVOKAWHGMBH-UHFFFAOYSA-N
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应用
4-己基间苯二酚用作合成有效的免疫抑制剂celastramycin A的原料。它是制备间苯二酚-sn -甘油衍生物的前体，对大麻素 1 类型受体表现出高亲和力。它也可以作为一个连接体，同时建立链状链。
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
388.4 °F
闪点(°C)
198 °C
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Yunbin Hao et al.
Molecules (Basel, Switzerland), 23(9) (2018-08-31)
A method for the rapid determination of 4-hexylresorcinol (4-HR) residue in shrimp by solid phase extraction (SPE) ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. 4-HR was extracted twice with methanol, and the extract was formulated into methanol-water solution
E Arias et al.
Journal of food science, 72(8), C422-C429 (2007-11-13)
The effects of ascorbic acid (AA) and 4-hexylresorcinol (4-HR) on pear polyphenoloxidase (PPO) activity and stability have been investigated in vitro. AA does not interact directly with PPO but prevents browning by reducing oxidized substrates. The 4-HR exerts a dual
4-Hexylresorcinol, a Potent Inhibitor of Mushroom Tyrosinase.
DAWLEY RM and FLURKEY WH.
Journal of Food Science, 58(3), 609-610 (1993)
Tobias Mann et al.
International journal of molecular sciences, 19(3) (2018-03-03)
Tyrosinase inhibitors are of great clinical interest as agents for the treatment of hyperpigmentary disorders; however, most compounds described in the literature lack clinical efficiency due to insufficient inhibitory activity against human tyrosinase (hTyr). Recently, we reported that thiazolyl resorcinols
Translational isomerizations in [2] catenanes with unsymmetrically substituted resorcinol-based tethers.
Halterman R L and Martyn D E
The Journal of Organic Chemistry, 72(21), 7841-7848 (2007)
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