跳轉至內容
Merck
全部照片(1)

重要文件

檢視所有文件

157457

Sigma-Aldrich

3,5-二叔丁基邻苯醌

98%

同義詞:

3,5-二叔丁基-1,2-苯醌, 3,5-二叔丁基-o-苯醌, 3,5-二叔丁基环己基-3,5-二烯-1,2-二酮, 3,5-二叔丁基苯醌, 3,5-双(1,1-二甲基乙基)-3,5-环己二烯-1,2-二酮, 4,6-二叔丁基-1,2-苯醌, 4,6-二叔丁基-o-苯醌

登入查看組織和合約定價
全部照片(1)

About This Item

線性公式:
[(CH3)3C]2C6H2(=O)2
CAS號碼:
3383-21-9
分子量：:
220.31
Beilstein:
2047944
EC號碼:
222-189-0
MDL號碼:
MFCD00001647
分類程式碼代碼:
12352100
PubChem物質ID:
24849680
NACRES:
NA.22
暫時無法取得訂價和供貨情況

品質等級

100

化驗

98%

形狀

solid

mp

112-114 °C (lit.)

SMILES 字串

CC(C)(C)C1=CC(=O)C(=O)C(=C1)C(C)(C)C

InChI

1S/C14H20O2/c1-13(2,3)9-7-10(14(4,5)6)12(16)11(15)8-9/h7-8H,1-6H3

InChI 密鑰

NOUZOVBGCDDMSX-UHFFFAOYSA-N

基因資訊

human ... ACHE(43) , BCHE(590) , CES1(1066)

尋找類似的產品？ 前往 產品比較指南

相關類別

一般說明

次膦基桥联络合物[[Fe2(η5-C5H5)2(μ-PR)(μ-CO)(CO)2] (R = Cy, Ph) 与3,5-二-叔-丁基-o-苯醌的反应已有报道。[1]

應用

3,5-二-叔-丁基-o-苯醌可用于制备苯并恶唑衍生物配体。[2]其可与无环二烯发生杂原子Diels Alder反应，制备1,4-苯二恶英。[3]

儲存類別代碼

11 - Combustible Solids

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

Eyeshields, Gloves, type N95 (US)

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
0000243793
0000246708
0000234429
MKCG5074
MKBW8205V

未看到正確版本？

如果您需要一個特定的版本，您可以透過批號來尋找特定憑證。

搜尋 COA

已經擁有該產品？

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

M Angeles Alvarez et al.
Dalton transactions (Cambridge, England : 2003), 41(48), 14498-14513 (2012-10-12)
The title complexes reacted readily with the methylating agents MeI and CF(3)SO(3)Me, chalcogens (O(2), S(8)) and borane adducts BH(3)·L (L = THF, N(t)Bu(3), PPh(3)) to initially give the corresponding neutral or cationic derivatives of the type [Fe(2)Cp(2){μ-P(E)R}(μ-CO)(CO)(2)](n) (Cp = η(5)-C(5)H(5);
Hitomi Tanaka et al.
International journal of molecular sciences, 19(10) (2018-09-27)
It is generally considered that eumelanin (EM) is photoprotective while pheomelanin (PM) is phototoxic. A recent study using a mouse model demonstrated that PM produces reactive oxygen species (ROS) that cause DNA damage and eventually lead to melanomagenesis. A biochemical
Hetero Diels-Alder reactions of 3, 5-di-tert-butyl-o-benzoquinone with acyclic dienes: novel synthesis of 1, 4-benzodioxines.
Nair V and Kumar S.
Journal of the Chemical Society. Chemical Communications, 11, 1341-1342 (1994)
Norma A Macías-Ruvalcaba et al.
The journal of physical chemistry. B, 110(43), 22043-22047 (2006-10-27)
The electrochemical reduction of 3,5-di-tert-butyl-1,2-benzoquinone, 1, has been studied in acetonitrile with added 2,2,2-trifluoroethanol, 2. At low concentrations of 2 the reaction proceeds by the following pathway: reduction of the quinone (Q) to its anion radical (Q*-) followed by complexation
Adám Kupán et al.
Journal of inorganic biochemistry, 103(3), 389-395 (2009-01-13)
The attempted alkylation of 1,3-bis(2'-pyridylimino)isoindoline (indH) by the use of n-BuLi and subsequent alkyl halides led to quaternization of the pyridine nitrogens and the zwitterionic monodentate N-ligand (Me(2)ind)I was formed. By the use of the ligand the copper(I) complex [Cu(I)(Me(2)ind)I(2)]
查看所有相關論文

Questions

Reviews

No rating value

Active Filters

我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務