Nome do produto：Diethyl Phosphite

Propriedades Computadas

• Massa Exacta: 137.09g/mol
• Carga de Superfície: 1
• XLogP3: 0.7
• Contagem de dadores de ligações de hidrogénio: 0
• Contagem de aceitadores de ligações de hidrogénio: 3
• Contagem de Ligações Rotativas: 4
• Massa monoisotópica: 137.036756g/mol
• Massa monoisotópica: 137.036756g/mol
• Superfície polar topológica: 35.5Ų
• Contagem de Átomos Pesados: 8
• Complexidade: 65.7
• Contagem de átomos isótopos: 0
• Contagem de Estereocentros Átomos Definidos: 0
• Contagem de Estereocentros Átomos Indefinidos: 0
• Contagem de Stereocenters de Obrigações Definidas: 0
• Contagem de Stereocenters Indefined Bond: 0
• Contagem de Unidades Ligadas Covalentemente: 1
• Contagem de Tautomeros: nothing
• Carga de Superfície: 1

Propriedades Experimentais

• Odor: Little odor
• Densidade do Vapor: 4.76 (Air = 1)
• Stability Shelf Life: Stable under recommended storage conditions.
• Decomposition: Hazardous decomposition products formed under fire conditions. - Carbon oxides, Oxides of phosphorus
• Viscosity: 1.13 centistokes at 25 °C
• LogP: 1.44910
• PSA: 59.00000
• Índice de Refracção: n20/D 1.407(lit.)
• Coeficiente de partição da água: Miscible (hydrolysis)
• Ponto de Fusão: -70 ºC
• Ponto de Flash: Fahrenheit: 179.6 ° f < br / > Celsius: 82 ° C < br / >
• Estabilidade/Prazo de validade: Stable. Incompatible with strong oxidizing agents, strong acids, acid chlorides, strong bases. May decompose on exposure to moisture. Combustible.
• Solubilidade: Soluble in water, tetrahydrofuran and ethanol.
• Sensibilidade: Moisture Sensitive

• Símbolo: GHS07
• RTECS：TG7875000
• WGK Alemanha：1
• Termo de segurança：S26;S37/39
• Instrução de Segurança：S26-S36/37/39-S37/39-S28-S27
• Frases de Risco：R36/37/38; R43
• Sinal de mercadorias perigosas： Xi
• Declaração de perigo：H315,H319,H335
• Declaração de Advertência：P261,P305+P351+P338
• Condição de armazenamento：Store in a cool, dry place. Keep container closed when not in use.
• Código da categoria de perigo：36/37/38
• Palavra de Sinal：Warning
• TSCA：Yes
• CÓDIGOS DA MARCA F FLUKA：10-13-21

• 1. A quaternary ammonium salt [H-dabco][AcO]: as a recyclable and highly efficient catalyst for the one-pot synthesis of β-phosphonomalonates Ya-Qin Yu,Da-Zhen Xu RSC Adv. 2015 5 28857
• 2. Synthesis of phosphonosulfonic acid building blocks as linkers for coordination polymers O. Beyer,T. Homburg,M. Albat,N. Stock,U. Lüning New J. Chem. 2017 41 8870
• 3. PC–N-Heterocycles: synthesis of biaryl-type 1,3-benzazaphospholes with ortho-substituted phenyl or 2-heteroaryl groups Bhaskar Reddy Aluri,Basit Niaz,Markus K. Kindermann,Peter G. Jones,Joachim Heinicke Dalton Trans. 2011 40 211
• 4. Synthesis by RAFT of innovative well-defined (co)polymers from a novel phosphorus-based acrylamide monomer Alain Graillot,Sophie Monge,Catherine Faur,Denis Bouyer,Jean-Jacques Robin Polym. Chem. 2013 4 795
• 5. Magnetic field controlled C60-TEMPO catalyst for the oxidation of alcohols Piotr Piotrowski,Jan ?ukrowski,Andrzej Kaim New J. Chem. 2020 44 1971
• 6. Inorganic base catalyzed synthesis of (2-amino-3-cyano-4H-chromene-4-yl) phosphonate derivatives via multi-component reaction under mild and efficient conditions Peng Dai,Gaofeng Zha,Xiaoyan Lai,Wei Liu,Qianwen Gan,Yongcun Shen RSC Adv. 2014 4 63420
• 7. Rational design of aminoanthraquinones for colorimetric detection of heavy metal ions in aqueous solution Elena Ranyuk,Alexei Uglov,Michel Meyer,Alla Bessmertnykh Lemeune,Franck Denat,Alexei Averin,Irina Beletskaya,Roger Guilard Dalton Trans. 2011 40 10491
• 8. Enantioselective chlorination and fluorination of β-keto phosphonates catalyzed by chiral Lewis acids Luca Bernardi,Karl Anker J?rgensen Chem. Commun. 2005 1324
• 9. 6-Polyamino-substituted quinolines: synthesis and multiple metal (CuII, HgII and ZnII) monitoring in aqueous media Anton S. Abel,Alexei D. Averin,Andrey V. Cheprakov,Vitaly A. Roznyatovsky,Franck Denat,Alla Bessmertnykh-Lemeune,Irina P. Beletskaya Org. Biomol. Chem. 2019 17 4243
• 10. Ordered SBA-15 mesoporous silica containing phosphonic acid groups prepared by a direct synthetic approach Robert J. P. Corriu,Lucien Datas,Yannick Guari,Ahmad Mehdi,Catherine Reyé,Chloé Thieuleux acid groups prepared by a direct synthetic approach. Robert J. P. Corriu Lucien Datas Yannick Guari Ahmad Mehdi Catherine Reyé Chloé Thieuleux Chem. Commun. 2001 763

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