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关于此项目
线性分子式:
(CH3)3CC6H3-1,2-(OH)2
化学文摘社编号:
分子量:
166.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-653-9
Beilstein/REAXYS Number:
2043335
MDL number:
Assay:
≥99.0%
Form:
powder
Quality Level
assay
≥99.0%
form
powder
bp
285 °C (lit.)
mp
52-55 °C (lit.), 56-58 °C
solubility
methanol: soluble 1 g/10 mL, clear, colorless
SMILES string
CC(C)(C)c1ccc(O)c(O)c1
InChI
1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
InChI key
XESZUVZBAMCAEJ-UHFFFAOYSA-N
General description
在酪氨酸酶的催化下,O2 存在下,4- 叔 -丁基邻苯二酚生成 4- 叔 -丁基- O -苯醌 。用循环伏安法和控制电位库仑法研究了 4--叔 -丁基邻苯二酚在 4-羟基香豆素存在下的电化学氧化。它通过阳极氧化进行电化学三聚反应,并利用循环伏安法和控制电位库仑法研究了三聚反应的机理 。
Application
- 自由基反应的抗氧化剂源:研究发现4-叔丁基儿茶酚可作为活性氢原子源用于自由基反应,特别是脱碘过程。说明它可用于有机合成化学(Povie et al., 2016)。
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Electrochemical study of 3, 4-dihydroxybenzoic acid and 4-tert-butylcatechol in the presence of 4-hydroxycoumarin application to the electro-organic synthesis of coumestan derivatives.
Golabi SM and Nematollahi D.
Journal of Electroanalytical Chemistry, 430(1), 141-146 (1997)
Mechanistic study of electrochemical oxidation of 4-tert-butylcatechol: A facile electrochemical method for the synthesis of new trimer of 4-tert-butylcatechol.
Nematollahi D, et al.
Electrochimica Acta, 49(15), 2495-2502 (2004)
Y Furukawa et al.
Biochemical pharmacology, 40(10), 2337-2342 (1990-11-15)
A series of 4-alkylcatechols and 1,2-diacetoxy-4-alkylbenzenes (from methyl to butyl) were chemically synthesized for in vitro evaluation as stimulators of nerve growth factor (NGF) synthesis. All compounds were proven to be potent in stimulating NGF synthesis in L-M cells (a
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 19671-100G | 04061838762207 |


