363596
Diethyl phosphoramidate
98%
동의어(들):
(Diethoxyphosphoryl)amine, Amidophosphoric acid diethyl ester, Diethyl amidophosphonate, Diethyl aminophosphonate, Diethyl phosphorylamide, O,O′-Diethylphosphoramidate
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모든 사진(1)
About This Item
Linear Formula:
H2NP(O)(OC2H5)2
CAS Number:
Molecular Weight:
153.12
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
98%
bp
140 °C/3 mmHg (lit.)
mp
51-53 °C (lit.)
SMILES string
CCOP(N)(=O)OCC
InChI
1S/C4H12NO3P/c1-3-7-9(5,6)8-4-2/h3-4H2,1-2H3,(H2,5,6)
InChI key
MCQILDHFZKTBOD-UHFFFAOYSA-N
일반 설명
Diethyl phosphoramidate is a chemical and biological toxin and its ultra-low level detection by Surface-Enhanced Raman Spectroscopy (SERS) is reported. It is reported as chemical warfare simulant.
애플리케이션
Diethyl phosphoramidate may be employed as reagent which mimics or imitates the actual chemical warfare agents. It may be used in the preparation of α-aminoalkyl phosphonates, via three-component Mannich type reaction.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Mehmet Yilmaz et al.
Physical chemistry chemical physics : PCCP, 16(12), 5563-5570 (2014-02-12)
The detection of molecules at an ultralow level by Surface-Enhanced Raman Spectroscopy (SERS) has recently attracted enormous interest for various applications especially in biological, medical, and environmental fields. Despite the significant progress, SERS systems are still facing challenges for practical
Surface-enhanced Raman scattering detection of chemical and biological agents using a portable Raman integrated tunable sensor.
Yan F and Vo-Dinh T.
Sensors and Actuators B, Chemical, 121(1), 61-66 (2007)
Surface detection of chemical warfare agent simulants and degradation products.
Kanu AB, et al.
Analytica Chimica Acta, 553(1), 148-159 (2001)
Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions-synthesis of N-phosphoramino a-aminophosphonates.
Zhang J, et al.
Green Chemistry, 9(12), 1341-1345 (2007)
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