Cas no 3722-74-5 (6-methyl-3,4-dihydro-2H-1-benzopyran)
6-methyl-3,4-dihydro-2H-1-benzopyran Chemical and Physical Properties
Names and Identifiers
-
- 6-methyl-3,4-dihydro-2H-chromene
- 2H-1-benzopyran, 3,4-dihydro-6-methyl-
- 6-Methylchromane
- SCHEMBL172501
- G34612
- AKOS033199373
- 6-methyl-3,4-dihydro-2H-1-benzopyran
- EN300-60319
- Z939648534
- CS-0252444
- 3722-74-5
- 6-methylchroman
-
- Inchi: 1S/C10H12O/c1-8-4-5-10-9(7-8)3-2-6-11-10/h4-5,7H,2-3,6H2,1H3
- InChI Key: IBUHLIDJSRXQFP-UHFFFAOYSA-N
- SMILES: O1C2C=CC(C)=CC=2CCC1
Computed Properties
- Exact Mass: 148.08886
- Monoisotopic Mass: 148.088815002g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 0
- Complexity: 133
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.6
- Topological Polar Surface Area: 9.2?2
Experimental Properties
- PSA: 9.23
6-methyl-3,4-dihydro-2H-1-benzopyran Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | FD01715-25g |
6-methylchromane |
3722-74-5 | 95% | 25g |
$1000 | 2023-09-07 | |
| TRC | M337103-5mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 5mg |
$ 50.00 | 2022-06-03 | ||
| TRC | M337103-10mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 10mg |
$ 65.00 | 2022-06-03 | ||
| TRC | M337103-50mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 50mg |
$ 95.00 | 2022-06-03 | ||
| A2B Chem LLC | AV56347-50mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 50mg |
$80.00 | 2024-04-20 | |
| A2B Chem LLC | AV56347-100mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 100mg |
$105.00 | 2024-04-20 | |
| A2B Chem LLC | AV56347-250mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 250mg |
$132.00 | 2024-04-20 | |
| A2B Chem LLC | AV56347-500mg |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 500mg |
$220.00 | 2024-04-20 | |
| A2B Chem LLC | AV56347-1g |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 1g |
$305.00 | 2024-04-20 | |
| A2B Chem LLC | AV56347-2.5g |
6-methyl-3,4-dihydro-2H-1-benzopyran |
3722-74-5 | 95% | 2.5g |
$565.00 | 2024-04-20 |
6-methyl-3,4-dihydro-2H-1-benzopyran Related Literature
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Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
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Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
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Marta Liras,Isabel Quijada-Garrido,Marta Palacios-Cuesta,Sonia Mu?oz-Durieux,Olga García Polym. Chem., 2014,5, 433-442
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
Additional information on 6-methyl-3,4-dihydro-2H-1-benzopyran
6-Methyl-3,4-Dihydro-2H-Chromene: A Comprehensive Overview
6-Methyl-3,4-dihydro-2H-chromene (CAS No. 3722-74-5) is a fascinating compound with a rich history and diverse applications in various fields. This compound, also referred to as chromene derivative, has garnered significant attention due to its unique chemical properties and potential uses in pharmaceuticals, agrochemicals, and materials science. In this article, we will delve into the structural characteristics, synthesis methods, applications, and recent advancements related to 6-methyl-3,4-dihydro-2H-chromene.
The structure of 6-methyl-3,4-dihydro-2H-chromene is characterized by a chromene skeleton with a methyl group at the 6-position. Chromenes are bicyclic compounds consisting of a benzene ring fused to a pyran ring. The dihydro form indicates that the pyran ring is partially saturated, giving the molecule its distinct properties. This compound is often studied for its ability to act as a precursor in the synthesis of more complex molecules, including those with potential pharmacological activity.
Recent research has focused on the synthesis of 6-methyl-3,4-dihydro-2H-chromene using various methodologies. One notable approach involves the use of Michael addition reactions, which allow for the construction of the chromene skeleton in a highly efficient manner. Additionally, advancements in catalytic asymmetric synthesis have enabled the preparation of enantiomerically enriched derivatives of this compound, opening new avenues for its application in drug discovery.
The applications of 6-methyl-3,4-dihydro-2H-chromene are vast and continually expanding. In the pharmaceutical industry, this compound serves as a valuable building block for the development of bioactive molecules. For instance, derivatives of this chromene have been investigated for their anti-inflammatory and antioxidant properties. Furthermore, 6-methyl-3,4-dihydro-2H-chromene has shown promise in agrochemicals as a potential herbicide or fungicide due to its ability to inhibit key enzymes involved in plant and fungal metabolism.
In materials science, chromene derivatives like 6-methyl-3,4-dihydro-2H-chromene are being explored for their photoresponsive properties. These compounds can undergo structural changes upon exposure to light, making them candidates for use in light-switchable materials and sensors. Recent studies have demonstrated that incorporating these chromenes into polymer matrices can enhance the mechanical and optical properties of the resulting materials.
From an environmental standpoint, researchers have also investigated the biodegradation pathways of 6-methyl-3,4-dihydro-2H-chromene to assess its potential impact on ecosystems. Studies indicate that this compound undergoes rapid degradation under aerobic conditions, reducing concerns about its persistence in the environment.
In conclusion, 6-methyl-3,4-dihydro-2H-chromene (CAS No. 3722-74-5) is a versatile compound with significant potential across multiple disciplines. Its unique chemical structure and diverse applications make it an area of continued interest for scientists and industry professionals alike. As research progresses, we can expect even more innovative uses for this remarkable compound.
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