157457
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
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About This Item
線性公式:
[(CH3)3C]2C6H2(=O)2
CAS號碼:
分子量：:
220.31
Beilstein:
2047944
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推薦產品
品質等級
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)
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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。
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。其可与无环二烯发生杂原子Diels Alder反应，制备1,4-苯二恶英。
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)
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A new method for the synthesis of fluorescent nucleosides has been developed. It has been shown that a reaction of benzoquinone with aminopropenyl group at C-5-position of 2'-deoxyuridine or 2'-deoxycytidine and aminopropynyl group at the C-7-position of 8-aza-7-deazaadenosine under extremely
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