Cas no 57332-84-0 (Ethyl a-Bromoethylglyoxalate)
Ethyl a-Bromoethylglyoxalate Chemical and Physical Properties
Names and Identifiers
-
- 3-Bromo-2-oxo-butyric acid ethyl ester
- Ethyl α-Bromoethylglyoxalate
- ethyl 2-oxo-3-bromobutyrate
- Ethyl 3-bromo-2-oxobutanoate
- Ethyl 3-bromo-2-oxobutyrate
- ethyl 3-bromo-2-oxovalerate
- ethyl dl-3-bromo-2-oxobutyrate
- methyl ethyl bromopyruvate
- QC-10762
- 3-Bromo-2-oxobutanoic acid ethyl ester
- Butanoic acid, 3-bromo-2-oxo-, ethyl ester
- Ethyl
- A-Bromoethylglyoxalate
- Ethyl-3-bromo-2-oxobutanoate
- SIOIQIWIQSMQAG-UHFFFAOYSA-N
- 5871AE
- WT82069
- 2-Oxo-3-bromobutyric acid ethyl ester
- AB0093519
- ST2404936
- 4CH
- CS-W006537
- Ethyl alpha-Bromoethylglyoxalate
- AKOS015997948
- DS-15483
- EN300-126200
- DTXSID00455814
- 57332-84-0
- SCHEMBL114311
- SY105905
- Ethyl a-Bromoethylglyoxalate
- 3-bromo-2-oxo-butyricacidethylester
- AMY202100100
- DB-017468
- MFCD19440735
- ALBB-022331
-
- MDL: MFCD19440735
- Inchi: 1S/C6H9BrO3/c1-3-10-6(9)5(8)4(2)7/h4H,3H2,1-2H3
- InChI Key: SIOIQIWIQSMQAG-UHFFFAOYSA-N
- SMILES: BrC(C)C(C(=O)OCC)=O
Computed Properties
- Exact Mass: 207.97351g/mol
- Monoisotopic Mass: 207.97351g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 4
- Complexity: 144
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 43.4
- XLogP3: 1.6
Experimental Properties
- Color/Form: No data avaiable
- Density: 1.474
- Melting Point: No data available
- Boiling Point: 213 oC
- Flash Point: 83 oC
- PSA: 43.37000
- LogP: 0.90200
- Vapor Pressure: 0.2±0.4 mmHg at 25°C
Ethyl a-Bromoethylglyoxalate Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
-
Warning Statement:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Ethyl a-Bromoethylglyoxalate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 080992-500mg |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 500mg |
4096.0CNY | 2021-06-30 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | B839309-1g |
3-Bromo-2-oxo-butyric acid ethyl ester |
57332-84-0 | 98% | 1g |
823.00 | 2021-05-17 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 080992-5g |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 5g |
17069CNY | 2021-05-08 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 080992-500mg |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 500mg |
4096CNY | 2021-05-08 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 080992-1g |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 1g |
5119CNY | 2021-05-08 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RZ181-100mg |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 90% | 100mg |
212CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RZ181-1g |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 90% | 1g |
864.0CNY | 2021-07-12 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RZ181-250mg |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 90% | 250mg |
466CNY | 2021-05-08 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RZ181-5g |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 90% | 5g |
3198.0CNY | 2021-07-12 | |
| TRC | E900300-500mg |
Ethyl a-Bromoethylglyoxalate |
57332-84-0 | 500mg |
$ 161.00 | 2023-09-07 |
Ethyl a-Bromoethylglyoxalate Related Literature
-
Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
-
Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
-
Robert P. Davies,Maria A. Giménez,Laura Patel,Andrew J. P. White Dalton Trans., 2008, 5705-5707
-
5. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
Additional information on Ethyl a-Bromoethylglyoxalate
Ethyl a-Bromoethylglyoxalate: A Comprehensive Overview
Ethyl a-Bromoethylglyoxalate, with the CAS number 57332-84-0, is a chemical compound that has garnered significant attention in recent years due to its unique properties and diverse applications. This compound, often referred to as Ethyl a-Bromoethylglyoxalate, belongs to the class of glyoxalates and is characterized by its brominated structure, which imparts distinctive reactivity and functionality. The compound's structure consists of a glyoxalate backbone with an ethyl group attached to the alpha position of the bromoethyl moiety, making it a valuable intermediate in organic synthesis.
Recent studies have highlighted the importance of Ethyl a-Bromoethylglyoxalate in various fields, including pharmaceuticals, agrochemicals, and materials science. Its ability to undergo nucleophilic substitution reactions has made it a key intermediate in the synthesis of bioactive molecules. For instance, researchers have utilized this compound to synthesize novel antibiotics and antifungal agents, leveraging its reactivity to create compounds with enhanced potency and selectivity.
The synthesis of Ethyl a-Bromoethylglyoxalate typically involves multi-step processes that require precise control over reaction conditions. One common approach involves the bromination of ethyl glyoxalate derivatives, followed by subsequent purification steps to ensure high purity. The compound's stability under various conditions has been extensively studied, with findings indicating that it is relatively stable under normal storage conditions but may decompose under harsh thermal or oxidative environments.
In terms of applications, Ethyl a-Bromoethylglyoxalate has found significant use in the development of advanced materials. Its ability to form stable covalent bonds makes it an ideal candidate for cross-linking polymers and developing high-performance adhesives. Recent advancements in polymer chemistry have demonstrated how this compound can be used to create materials with improved mechanical properties and thermal stability.
Another area where Ethyl a-Bromoethylglyoxalate has shown promise is in catalysis. Researchers have explored its potential as a catalyst in various organic reactions, particularly those involving nucleophilic substitution and addition mechanisms. Its role as a catalyst has been validated through numerous experiments, where it has been shown to significantly accelerate reaction rates while maintaining high selectivity.
From an environmental perspective, understanding the fate and transport of Ethyl a-Bromoethylglyoxalate is crucial for ensuring its safe use and disposal. Studies have indicated that the compound undergoes biodegradation under aerobic conditions, with microbial activity playing a significant role in its breakdown. However, further research is needed to fully characterize its environmental impact and develop strategies for minimizing ecological risks.
In conclusion, Ethyl a-Bromoethylglyoxalate (CAS No: 57332-84-0) is a versatile compound with wide-ranging applications across multiple disciplines. Its unique chemical properties make it an invaluable tool in organic synthesis, catalysis, and materials science. As research continues to uncover new potential uses for this compound, it is likely to play an even more prominent role in advancing scientific and technological innovations.
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