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About This Item
经验公式(希尔记法):
C6H10F3NO2
CAS号:
分子量:
185.14
Beilstein:
6644043
MDL编号:
UNSPSC代码:
12352202
PubChem化学物质编号:
NACRES:
NA.22
方案
≥98.0% (GC)
表单
liquid
反应适用性
reagent type: cross-linking reagent
折射率
n20/D 1.413
密度
1.262 g/mL at 20 °C (lit.)
官能团
hydroxyl
SMILES字符串
O=C(NCCCCO)C(F)(F)F
InChI
1S/C6H10F3NO2/c7-6(8,9)5(12)10-3-1-2-4-11/h11H,1-4H2,(H,10,12)
InChI key
LZUDPIMZEXACCH-UHFFFAOYSA-N
其他说明
向柔红酮中引入 4-氨基丁基残基,以形成与 DNA 的最佳嵌合的结构单元;磷酸二酯中的保护基团;通过环去酯化反应发生裂解
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
A. Wilk et al.
The Journal of Organic Chemistry, 62, 6712-6712 (1997)
Zoltán Dienes et al.
The Journal of organic chemistry, 61(20), 6958-6970 (1996-10-04)
The BF(3).Et(2)O-promoted Diels-Alder addition of 1-acetylvinyl RADO(Et)-ate (RADO(Et)-ate = 3-ethyl-2-oxo-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-exo-carboxylate) to 1-(dimethoxymethyl)-2,3,5,6-tetramethylidene-7-oxabicyclo[2.2.1]heptane led to one major monoadduct that added to 1,2-didehydrobenzene and was converted into (-)-4-demethoxy-7-deoxydaunomycinone and (2R)-12-acetoxy-2-acetyl-5-(bromomethyl)-1,2,3,4-tetrahydronaphthacen-2-yl RADO(Et)-ate. The latter compound was used to construct (8R)-8-acetyl-6,8-dihydroxy-11-[[(3'-[(aminopropyl)oxy]-, -4'-[(aminobutyl)oxy], and -5'-[(aminopentyl)oxy]methyl]-7,8,9,10-tetrahydronaphthacene-5,12-dione
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