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化驗
97%
mp
72-76 °C (lit.)
SMILES 字串
Cc1ccc(Cl)cc1O
InChI
1S/C7H7ClO/c1-5-2-3-6(8)4-7(5)9/h2-4,9H,1H3
InChI 密鑰
KKFPXGXMSBBNJI-UHFFFAOYSA-N
一般說明
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.
應用
5-Chloro-2-methylphenol may be used in the synthesis of 4-chlorosalicylaldehyde triacetate and 1-chloro-3-isopropoxy-4-methylbenzene.
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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)
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)
Hydroxylation of para-chlorotoluene by model complexes of cytochrome P-450.
Sakurai H, et al.
Inorgorganica Chimica Acta, 91(4), 233-236 (1984)
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