D45800
3,5-二叔丁基儿茶酚
98%
别名:
3,5-二叔丁基-1,2-二羟基苯, 3,5-二叔丁基-1,2-苯二醇, 3,5-二叔丁基邻氢醌, 3,5-二叔丁基邻苯二酚, 3,5-双(1,1-二甲基乙基)-1,2-苯二醇, 4,6-二叔丁基-1,2-苯二醇, 4,6-二叔丁基邻苯二酚
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关于此项目
线性分子式:
[(CH3)3C]2C6H2-1,2-(OH)2
化学文摘社编号:
分子量:
222.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-816-9
Beilstein/REAXYS Number:
1370212
MDL number:
产品名称
3,5-二叔丁基儿茶酚, 98%
InChI
1S/C14H22O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8,15-16H,1-6H3
InChI key
PJZLSMMERMMQBJ-UHFFFAOYSA-N
SMILES string
CC(C)(C)c1cc(O)c(O)c(c1)C(C)(C)C
assay
98%
form
crystals
mp
95-100 °C (lit.)
Quality Level
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Application
3,5-二-叔丁基儿茶酚可用作：
- 通过催化氧化制备3,5-二-叔-丁基醌的反应物。
- 苯乙烯和丁二烯等单体生产中的聚合抑制剂。
- 以L-脯氨酸为催化剂通过不对称亚硝基羟醛缩反应合成对映选择性 1,2-恶嗪烷和异恶唑烷的添加剂。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Mehmet Tümer et al.
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In this study, we synthesized the amine compound 2-(2-aminoethyliminomethyl)phenol (H(3)A) as the starting material, and then we prepared the polydentate Schiff base ligands from the reactions of the amine compound (H(3)A) with phtaldialdehyde (H(2)L), 4-methyl-2,6-di-formlyphenol (H(3)L(1)) and 4-t-butyl-2,6-di-formylphenol (H(3)L(2)) in
Structural correlation of catecholase-like activities of oxy-bridged dinuclear copper(II) complexes.
C H Kao et al.
Journal of inorganic biochemistry, 84(3-4), 171-178 (2001-05-26)
Eight oxy-bridged dinuclear copper(II) complexes with catecholase-like sites, [Cu(L1)X]2 (HL1 = 1-diethylaminopropan-2-ol, X=N3- 1, NCO- 2, and NO2- 3), [Cu(L2)X]2 (HL2=N-ethylsalicylaldimine, X=NO3- 4, Cl- 5, N3- 6, NCS- 7), and [Cu(L3)]2(ClO4)2, 8 (HL3=N-(salicylidene)-N'-(2-pyridylaldene)propanediamine) have been prepared and characterized. The single
Apurba Biswas et al.
Inorganic chemistry, 51(15), 7993-8001 (2012-07-05)
Three double phenoxido-bridged dinuclear nickel(II) complexes, namely [Ni(2)(L(1))(2)(NCS)(2)] (1), [Ni(2)(L(2))(2)(NCS)(2)] (2), and [Ni(2)(L(3))(2)(NCS)(2)] (3) have been synthesized using the reduced tridentate Schiff-base ligands 2-[1-(3-methylamino-propylamino)-ethyl]-phenol (HL(1)), 2-[1-(2-dimethylamino-ethylamino)-ethyl]-phenol (HL(2)), and 2-[1-(3-dimethylamino-propylamino)-ethyl]-phenol (HL(3)), respectively. The coordination compounds have been characterized by X-ray structural
Christopher Grieco et al.
Faraday discussions, 216(0), 520-537 (2019-04-24)
Eumelanin is a natural pigment with photoprotective and radical scavenging characteristics, which are vital for a multitude of living organisms. However, the molecular mechanisms behind these functions remain obscure, in part because eumelanin is a heterogeneous polymer composed of a
Catalytic oxidation of 3, 5-di-tert-butylcatechol by a manganese (III) 18-azametallacrown-6 compound: Synthesis, crystal structure, fluorescence, magnetic and kinetic investigation
Majumder A, et al.
Inorganica chimica acta, 359(8), 2375-2382 (2006)
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