Cas no 13638-89-6 (meso-2,3-Diphenyl-succinic Acid Diethyl Ester)
meso-2,3-Diphenyl-succinic Acid Diethyl Ester Chemical and Physical Properties
Names and Identifiers
-
- diethyl (2R,3S)-2,3-diphenylbutanedioate
- Butanedioic acid, 2,3-diphenyl-, diethyl ester, (2R,3S)-
- Diethyl (2R,3S)-2,3-diphenylsuccinate
- LogP
- MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER
- meso-2,3-Diphenyl-succinic Acid Diethyl Ester
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- Inchi: 1S/C20H22O4/c1-3-23-19(21)17(15-11-7-5-8-12-15)18(20(22)24-4-2)16-13-9-6-10-14-16/h5-14,17-18H,3-4H2,1-2H3/t17-,18+
- InChI Key: AMAMWUWLDQUKAP-HDICACEKSA-N
- SMILES: O(CC)C([C@H](C1C=CC=CC=1)[C@@H](C(=O)OCC)C1C=CC=CC=1)=O
Computed Properties
- Exact Mass: 326.15186
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 24
- Rotatable Bond Count: 9
Experimental Properties
- PSA: 52.6
meso-2,3-Diphenyl-succinic Acid Diethyl Ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D494048-100mg |
meso-2,3-Diphenyl-succinic Acid Diethyl Ester |
13638-89-6 | 100mg |
$ 50.00 | 2022-06-05 | ||
| TRC | D494048-500mg |
meso-2,3-Diphenyl-succinic Acid Diethyl Ester |
13638-89-6 | 500mg |
$ 70.00 | 2022-06-05 | ||
| TRC | D494048-1g |
meso-2,3-Diphenyl-succinic Acid Diethyl Ester |
13638-89-6 | 1g |
$ 115.00 | 2022-06-05 | ||
| Fluorochem | 046212-10g |
meso-2,3-Diphenyl-succinic acid diethyl ester |
13638-89-6 | >98 | 10g |
£123.00 | 2022-02-28 | |
| Fluorochem | 046212-50g |
meso-2,3-Diphenyl-succinic acid diethyl ester |
13638-89-6 | >98 | 50g |
£408.00 | 2022-02-28 | |
| Crysdot LLC | CD12148502-100g |
meso-2,3-Diphenyl-succinic acid diethyl ester |
13638-89-6 | 95+% | 100g |
$774 | 2024-07-23 |
meso-2,3-Diphenyl-succinic Acid Diethyl Ester Related Literature
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
-
Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
Additional information on meso-2,3-Diphenyl-succinic Acid Diethyl Ester
Professional Introduction to Meso-2,3-Diphenyl-succinic Acid Diethyl Ester (CAS No. 13638-89-6)
Meso-2,3-Diphenyl-succinic Acid Diethyl Ester, a compound with the chemical formula C??H??O?, is a significant molecule in the field of organic chemistry and pharmaceutical research. This compound, identified by its unique CAS number 13638-89-6, has garnered attention due to its structural properties and potential applications in various scientific domains.
The molecular structure of Meso-2,3-Diphenyl-succinic Acid Diethyl Ester consists of a central succinic acid backbone substituted with two phenyl groups at the 2 and 3 positions, further modified by diethyl ester groups. This configuration imparts specific chemical characteristics that make it a valuable intermediate in synthetic chemistry. The presence of aromatic rings enhances its reactivity and interaction with biological systems, making it a candidate for drug development and material science applications.
In recent years, the compound has been explored for its potential in pharmaceutical applications. Researchers have been particularly interested in its role as a precursor in the synthesis of more complex molecules. The phenyl groups in its structure allow for further functionalization, enabling the creation of derivatives with tailored properties. These derivatives could potentially serve as inhibitors or modulators in therapeutic contexts.
One of the most promising areas of research involving Meso-2,3-Diphenyl-succinic Acid Diethyl Ester is its application in the development of novel materials. The compound's ability to form stable complexes with other molecules makes it useful in creating polymers and coatings with enhanced mechanical and chemical properties. These materials could find applications in industries ranging from electronics to automotive manufacturing.
The synthesis of Meso-2,3-Diphenyl-succinic Acid Diethyl Ester is another area where significant advancements have been made. Modern synthetic techniques have allowed for more efficient and scalable production methods. These improvements have not only reduced costs but also increased the availability of the compound for research purposes. This accessibility has spurred further investigation into its potential uses.
In academic research, Meso-2,3-Diphenyl-succinic Acid Diethyl Ester has been used as a model compound to study reaction mechanisms and develop new synthetic strategies. Its well-defined structure provides a scaffold for testing various chemical transformations. By understanding how this compound behaves under different conditions, scientists can gain insights that are applicable to broader areas of organic chemistry.
The pharmaceutical industry has also shown interest in exploring the therapeutic potential of derivatives of Meso-2,3-Diphenyl-succinic Acid Diethyl Ester. Initial studies suggest that certain modifications to its structure could lead to compounds with anti-inflammatory or anti-cancer properties. While these findings are still in the early stages of research, they highlight the compound's versatility and its potential as a building block for future drug candidates.
The environmental impact of synthesizing and using Meso-2,3-Diphenyl-succinic Acid Diethyl Ester is another consideration that researchers are addressing. Efforts are being made to develop greener synthetic routes that minimize waste and reduce energy consumption. These sustainable practices are essential for ensuring that the production of such compounds aligns with global environmental goals.
In conclusion, Meso-2,3-Diphenyl-succinic Acid Diethyl Ester (CAS No. 13638-89-6) is a multifaceted compound with significant potential in both pharmaceuticals and materials science. Its unique structure and reactivity make it a valuable tool for researchers across various disciplines. As scientific understanding continues to evolve, it is likely that new applications for this compound will emerge, further solidifying its importance in modern chemistry.
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