Cas no 34170-88-2 (Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1))
Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1) Chemical and Physical Properties
Names and Identifiers
-
- Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1)
- potassium,2-dimethoxyphosphorylacetate
- P,P-Dimethylphosphonoacetic acid potassium salt
- Phosphonoacetic acid P,P-dimethyl ester potassium salt
- potassium (dimethylphosphono)acetate
- Potassium P,P-dimethylphosphonoacetate
- POTASSIUM 2-(DIMETHOXYPHOSPHORYL)ACETATE
- J-019476
- potassium;2-dimethoxyphosphorylacetate
- 34170-88-2
- Potassium (dimethoxyphosphoryl)acetate
- FT-0712289
- WPDZWGGYOFPQEO-UHFFFAOYSA-M
- DTXSID40635390
-
- Inchi: 1S/C4H9O5P.K/c1-8-10(7,9-2)3-4(5)6;/h3H2,1-2H3,(H,5,6);/q;+1/p-1
- InChI Key: WPDZWGGYOFPQEO-UHFFFAOYSA-M
- SMILES: [K+].P(CC(=O)[O-])(=O)(OC)OC
Computed Properties
- Exact Mass: 205.97500
- Monoisotopic Mass: 205.97464183g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 11
- Rotatable Bond Count: 4
- Complexity: 162
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 75.7?2
Experimental Properties
- Melting Point: 113-115?°C
- PSA: 85.47000
- LogP: -0.77780
Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1) Customs Data
- HS CODE:2931900090
- Customs Data:
China Customs Code:
2931900090Overview:
2931900090. Other organic-Inorganic compound. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:6.5%. general tariff:30.0%
Summary:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%
Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1) Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHENG KE LU SI SHENG WU JI SHU | sc-255447-5 g |
Potassium P,P-dimethylphosphonoacetate, |
34170-88-2 | 5g |
¥361.00 | 2023-07-11 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-255447-5g |
Potassium P,P-dimethylphosphonoacetate, |
34170-88-2 | 5g |
¥361.00 | 2023-09-05 |
Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1) Related Literature
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Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
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Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
Additional information on Acetic acid,2-(dimethoxyphosphinyl)-, potassium salt (1:1)
Acetic Acid, 2-(Dimethoxyphosphinyl)-, Potassium Salt (1:1): A Comprehensive Overview
The compound with CAS No 34170-88-2, commonly referred to as Acetic acid, 2-(dimethoxyphosphinyl)-, potassium salt (1:1), is a versatile and significant chemical entity in the field of organic synthesis and materials science. This compound has garnered attention due to its unique structural properties and its potential applications in various industries. Recent advancements in chemical research have further highlighted its role in modern synthetic methodologies.
The molecular structure of Acetic acid, 2-(dimethoxyphosphinyl)-, potassium salt (1:1) consists of a potassium ion (K+) and an acetic acid derivative with a dimethoxyphosphinyl group attached at the beta position. This structure imparts the compound with distinctive reactivity and stability, making it a valuable intermediate in the synthesis of complex organic molecules. The dimethoxyphosphinyl group introduces unique electronic properties that facilitate various catalytic transformations.
Recent studies have demonstrated the utility of this compound in asymmetric catalysis, particularly in the synthesis of chiral centers. Its ability to act as a ligand in transition metal-catalyzed reactions has been extensively explored. For instance, researchers have employed this compound in the enantioselective synthesis of bioactive molecules, showcasing its potential in drug discovery and development.
In addition to its catalytic applications, Acetic acid, 2-(dimethoxyphosphinyl)-, potassium salt (1:1) has found relevance in materials science. Its phosphorus-containing structure makes it a candidate for use in flame retardants and high-performance polymers. Recent breakthroughs in polymer chemistry have highlighted its role as a building block for advanced materials with tailored mechanical and thermal properties.
The synthesis of this compound involves a multi-step process that typically begins with the preparation of the corresponding acetic acid derivative followed by its conversion into the potassium salt form. The reaction conditions are carefully optimized to ensure high yields and purity. Researchers have also explored alternative synthetic routes to enhance scalability and reduce production costs.
From an environmental perspective, the compound's biodegradability and eco-friendly properties are under investigation. Preliminary studies suggest that it exhibits moderate biodegradation rates under aerobic conditions, which is a positive indicator for its sustainable use in industrial applications.
In conclusion, Acetic acid, 2-(dimethoxyphosphinyl)-, potassium salt (1:1) is a multifaceted chemical entity with significant potential across diverse fields. Its unique structure, coupled with recent advancements in synthetic methodologies and application-oriented research, positions it as a key player in contemporary chemical innovation.
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