281069
Azetidine
98%
동의어(들):
Trimethylene imine
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C3H7N
CAS 번호:
Molecular Weight:
57.09
Beilstein:
102384
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
분석
98%
양식
liquid
refractive index
n20/D 1.432 (lit.)
bp
61-62 °C (lit.)
density
0.847 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
C1CNC1
InChI
1S/C3H7N/c1-2-4-3-1/h4H,1-3H2
InChI key
HONIICLYMWZJFZ-UHFFFAOYSA-N
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관련 카테고리
일반 설명
Phototransformations of azetidine radical cations in freonic matrices under the action of light with λ = 436nm has been investigated. The IR spectrum of azetidine in solid argon matrices has been measured.
애플리케이션
Azetidine was employed in:
- a high yielding palladium-catalyzed cross-coupling raection with aryl bromides
- Ullmann type coupling reaction with iodonitroflourenes
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-4.0 °F
Flash Point (°C)
-20 °C
개인 보호 장비
Faceshields, Gloves, Goggles
Synthesis, 243-243 (2007)
Synthesis, 3245-3245 (2006)
Phototransformations of azetidine radical cations stabilized in freonic matrices.
Sorokin ID, et al.
High Energy Chemistry, 48(3), 180-184 (2014)
Experimental and computational studies of the structure and vibrational spectra of azetidine derivatives.
Thompson CA, et al.
Journal of Molecular Structure, 491(1), 67-80 (1999)
Niamh M O'Boyle et al.
European journal of medicinal chemistry, 46(9), 4595-4607 (2011-08-16)
The structure-activity relationships of antiproliferative β-lactams, focusing on modifications at the 4-position of the β-lactam ring, is described. Synthesis of this series of compounds was achieved utilizing the Staudinger and Reformatsky reactions. The antiproliferative activity was assessed in MCF-7 cells
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