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About This Item
線性公式:
(CH3)3CCOCH2CN
CAS號碼:
分子量：:
125.17
Beilstein:
1746674
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
99%
形狀
solid
bp
125-126 °C/22 mmHg (lit.)
mp
66-69 °C (lit.)
SMILES 字串
CC(C)(C)C(=O)CC#N
InChI
1S/C7H11NO/c1-7(2,3)6(9)4-5-8/h4H2,1-3H3
InChI 密鑰
MXZMACXOMZKYHJ-UHFFFAOYSA-N
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應用
4,4-Dimethyl-3-oxopentanenitrile has been used in the preparation of:
- 4,4-dimethyl-3-oxo-2-benzylpentanenitrile[1]
- 4,4-dimethyl-3-oxo-2-(4-hydroxybenzyl)pentanenitrile[1]
- 4,4-dimethyl-3-oxo-2-(4-methoxybenzyl)pentanenitrile[1]
- 4,4-dimethyl-3-oxo-2-(4-fluorobenzyl)pentanenitrile[1]
- 4,4-dimethyl-3-oxo-2-(3,4-methylenedioxybenzyl)pentanenitrile[1]
- 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-phenylurea[2]
訊號詞
Danger
危險聲明
防範說明
危險分類
Acute Tox. 3 Oral
儲存類別代碼
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
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, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
John Regan et al.
Journal of medicinal chemistry, 45(14), 2994-3008 (2002-06-28)
We report on a series of N-pyrazole, N'-aryl ureas and their mode of binding to p38 mitogen activated protein kinase. Importantly, a key binding domain that is distinct from the adenosine 5'-triphoshate (ATP) binding site is exposed when the conserved
Phillip J Black et al.
Organic & biomolecular chemistry, 4(1), 116-125 (2005-12-17)
Alcohols have been employed as substrates for C-C bond-forming reactions which involve initial activation by the temporary removal of hydrogen to form an aldehyde. The intermediate aldehyde is converted into an alkene via a Horner-Wadsworth-Emmons reaction, nitroaldol and aldol reactions.
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