추천 제품
분석
99%
형태
solid
bp
125-126 °C/22 mmHg (lit.)
mp
66-69 °C (lit.)
SMILES string
CC(C)(C)C(=O)CC#N
InChI
1S/C7H11NO/c1-7(2,3)6(9)4-5-8/h4H2,1-3H3
InChI key
MXZMACXOMZKYHJ-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
4,4-Dimethyl-3-oxopentanenitrile has been used in the preparation of:
- 4,4-dimethyl-3-oxo-2-benzylpentanenitrile
- 4,4-dimethyl-3-oxo-2-(4-hydroxybenzyl)pentanenitrile
- 4,4-dimethyl-3-oxo-2-(4-methoxybenzyl)pentanenitrile
- 4,4-dimethyl-3-oxo-2-(4-fluorobenzyl)pentanenitrile
- 4,4-dimethyl-3-oxo-2-(3,4-methylenedioxybenzyl)pentanenitrile
- 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-phenylurea
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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
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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