推荐产品
质量水平
方案
97%
mp
72-76 °C (lit.)
官能团
chloro
SMILES字符串
Cc1ccc(Cl)cc1O
InChI
1S/C7H7ClO/c1-5-2-3-6(8)4-7(5)9/h2-4,9H,1H3
InChI key
KKFPXGXMSBBNJI-UHFFFAOYSA-N
一般描述
5-Chloro-2-methylphenol (5-chloro-o-cresol) can be synthesized from 5-chloro-2-methylaniline. 5-Chloro-2-methylphenol is formed as one of the hydroxylation reaction products of p-chlorotoluene.
应用
5-Chloro-2-methylphenol may be used in the synthesis of 4-chlorosalicylaldehyde triacetate and 1-chloro-3-isopropoxy-4-methylbenzene.
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
A synthesis of micandrol-C a novel methylthiophenanthrenediol isolated from the trunkwood of Micandropsis scleroxylon.
Sargent MV and Zwicky AB.
Journal of the Chemical Society. Perkin Transactions 1, 6, 1713-1715 (1990)
Hydroxylation of para-chlorotoluene by model complexes of cytochrome P-450.
Sakurai H, et al.
Inorgorganica Chimica Acta, 91(4), 233-236 (1984)
Coordination in Solutions. II. Acid Dissociation Constants in Water and Structural Reassignments of the Isomeric Chlorosalicylaldehydes1, 2.
Postmus Jr C, et al.
The Journal of Organic Chemistry, 29(9), 233-236 (1984)
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