추천 제품
Quality Level
분석
98%
bp
106 °C/15 mmHg (lit.)
mp
74-76 °C (lit.)
solubility
chloroform: very soluble(lit.)
ethanol: very slightly soluble(lit.)
water: very soluble(lit.)
저장 온도
2-8°C
SMILES string
O=C1CCN1
InChI
1S/C3H5NO/c5-3-1-2-4-3/h1-2H2,(H,4,5)
InChI key
MNFORVFSTILPAW-UHFFFAOYSA-N
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일반 설명
2-Azetidinone is an unsubstituted four membered lactam. 2-Azetidinone is the fundamental building block of β-lactam antibiotics. X-ray photoelectron spectra of 2-azetidinone was investigated. 2-Azetidinone undergoes hydrolysis with aqueous alkali to yield β-alanine.
애플리케이션
2-Azetidinone was used in synthesis of optically pure densely functionalized γ-lactams.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
The Journal of organic chemistry, 69(3), 993-996 (2004-01-31)
A synthesis of optically pure densely functionalized gamma-lactams starting from 2-azetidinone-tethered iminophosphoranes has been developed. Full chirality transfer has been accomplished from the enantiomerically pure 2-azetidinones. The addition of lithium acetylides to 4-oxoazetidine-2-carbaldehydes at -78 degrees C smoothly yielded propargylic
Investigation of the molecular structure and VUV-induced ion dissociation dynamics of 2-azetidinone (C3 H5 NO).
Rapid communications in mass spectrometry : RCM, 35(3), e8988-e8988 (2020-10-24)
2-Azetidinone (?-propiolactam)
Journal of the American Chemical Society, 71(6), 2129-2131 (1949)
The journal of physical chemistry. A, 116(33), 8653-8660 (2012-07-18)
X-ray photoelectron spectra of the core and valence levels of the fundamental building blocks of β-lactam antibiotics have been investigated and compared with theoretical calculations. The spectra of the compounds 2-azetidinone and the 2- and 4-isomers of thiazolidine-carboxylic acid are
Bioorganic & medicinal chemistry, 23(3), 632-647 (2015-01-01)
The prevalence of drug resistance in both clinical and community settings as a consequence of alterations of biosynthetic pathways, enzymes or cell wall architecture is a persistent threat to human health. We have designed, synthesized, and tested a novel class
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