144134
3,5-二甲基苯酚
≥99%
别名:
5-羟基间二甲苯, 对称间二甲苯酚
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关于此项目
线性分子式:
(CH3)2C6H3OH
化学文摘社编号:
分子量:
122.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-606-5
Beilstein/REAXYS Number:
774117
MDL number:
Assay:
≥99%
Form:
fibers, solid
InChI key
TUAMRELNJMMDMT-UHFFFAOYSA-N
InChI
1S/C8H10O/c1-6-3-7(2)5-8(9)4-6/h3-5,9H,1-2H3
SMILES string
Cc1cc(C)cc(O)c1
assay
≥99%
form
fibers, solid
bp
222 °C (lit.)
Quality Level
mp
65-66 °C
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Application
3,5-二甲基苯酚用于通过毛细管气相色谱法同时测定苯酚，邻-，对-，间-甲酚，1-，2-萘酚和二甲酚异构体的尿浓度。它被用作全合成 landomycin A 的起始试剂，landomycin A 是最有效的抗肿瘤血管生成素抗生素和光学活性聚丙酸酯单元。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 2
flash_point_f
179.6 °F
flash_point_c
82 °C
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
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Takashi Sugimura et al.
Organic letters, 6(24), 4439-4442 (2004-11-19)
Optically active polypropionate units were synthesized in 9-11 steps from 3,5-dimethylphenol. The sequence consists of the Buchner reaction controlled by a chiral 2,4-pentanediol tether and diastereoselective hydrogenation over Raney nickel. [reaction: see text]
Xiaoyu Yang et al.
Journal of the American Chemical Society, 133(32), 12433-12435 (2011-07-26)
The first total synthesis of landomycin A, the longest and most potent antitumor angucycline antibiotic, has been achieved in 63 steps and 0.34% overall yield starting from 2,5-dihydroxybenzoic acid, 3,5-dimethylphenol, triacetyl d-glucal, and d-xylose, with a convergent linear sequence of
G Bieniek
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An attempt was made to establish a method for the simultaneous determination of urinary concentrations of phenol, o-, p- and m-cresols, 1- and 2-naphthol and xylenol isomers by capillary gas chromatography. Urine samples were extracted after acid hydrolysis of glucuronides
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E C Cole et al.
Journal of applied microbiology, 95(4), 664-676 (2003-09-13)
To describe the relationship between antibiotic and antibacterial resistance in environmental and clinical bacteria from home environments across geographical locations, relative to the use or nonuse of antibacterial products, with a focus on target organisms recognized as potential human pathogens.
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