Dimethyl phenylphosphonite - ≥98% , CAS No.2946-61-4

CAS: 2946-61-4 Cat. No.: D189099 Fórmula: C₆H₅P(OCH₃)₂ Peso molecular: 170.15 Número CE: 220-960-6

GRADE & PURITY ≥98%

Synonyms

FT-0625042 | J-017531 | Phosphonous acid, P-phenyl-, dimethyl ester | D5014 | dimethoxy(phenyl)phosphane | Phosphonous acid, phenyl-, dimethyl ester | EINECS 220-960-6 | AKOS004908691 | Dimethoxyphenylphosphine | SCHEMBL196040 | CAA94661 | UNII-9AN05LG4JZ

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

FT-0625042 | J-017531 | Phosphonous acid, P-phenyl-, dimethyl ester | D5014 | dimethoxy(phenyl)phosphane | Phosphonous acid, phenyl-, dimethyl ester | EINECS 220-960-6 | AKOS004908691 | Dimethoxyphenylphosphine | SCHEMBL196040 | CAA94661 | UNII-9AN05LG4JZ

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥98%

Nomes e identificadores

• Pubchem Sid: 488185239
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185239
• Sorrisos canónicos: COP(C1=CC=CC=C1)OC
• IUPAC Name: dimethoxy(phenyl)phosphane
• InChIKey: LMZLQYYLELWCCW-UHFFFAOYSA-N
• INCHI: 1S/C8H11O2P/c1-9-11(10-2)8-6-4-3-5-7-8/h3-7H,1-2H3
• SMILES isoméricas: COP(C1=CC=CC=C1)OC
• WGK Alemanha: 3
• Peso molecular: 170.15
• Reaxy-Rn: 1073018
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1073018&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organopnictogen compounds Organophosphorus compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriedades químicas e físicas

• Solubilidade: Miscible with alcohol. Immiscible with water.
• Sensibilidade: Heat sensitive; Air sensitive
• Índice de refração: 1.53
• Ponto de inflamação (°F): 235.4 °F
• Ponto de inflamação (°C): 81℃
• Ponto de ebulição (°C): 194 ℃
• Peso molecular: 170.150 g/mol
• XLogP3: 1.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 170.05 Da
• Monoisotopic Mass: 170.05 Da
• Topological Polar Surface Area: 18.500 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 98.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referências

1. Lin Huang, Wantao Wang, Yiwen Xian, Lei Liu, Jinghao Fan, Hongmei Liu, Zhaomin Zheng, Decheng Wu.  (2023)  Rapidly in situ forming an injectable Chitosan/PEG hydrogel for intervertebral disc repair.  Materials Today Bio,      [PMID:37576872] [10.1016/j.mtbio.2023.100752]

2. Yuandou Wang, Shuxin Wang, Wenju Hu, Feng Su, Fusheng Liu, Suming Li.  (2022)  In situ photo-crosslinked hydrogels prepared from acrylated 4-arm-poly(ethylene glycol)-poly(ε-caprolactone) block copolymers for local cancer therapy.  POLYMERS FOR ADVANCED TECHNOLOGIES,  33  (8): (2620-2631).  [PMID:] [10.1002/pat.5718]