Cas no 153654-07-0 (methyl methoxy(methyl)carbamate)
methyl methoxy(methyl)carbamate Chemical and Physical Properties
Names and Identifiers
-
- methyl methoxy(methyl)carbamate
- CS-W001820
- Methylmethoxy(methyl)carbamate
- 153654-07-0
- methyl N-methoxy-N-methylcarbamate
- SCHEMBL8773016
- s11702
- AKOS026732156
- N-Carbomethoxy-N-methoxymethylamine
- Methyl methoxy(methyl)carbamate #
- MFCD19686570
-
- Inchi: 1S/C4H9NO3/c1-5(8-3)4(6)7-2/h1-3H3
- InChI Key: XMRDNYNZIUDSIR-UHFFFAOYSA-N
- SMILES: O(C)N(C(=O)OC)C
Computed Properties
- Exact Mass: 119.058243149g/mol
- Monoisotopic Mass: 119.058243149g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 8
- Rotatable Bond Count: 2
- Complexity: 83.4
- 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: 0.2
- Topological Polar Surface Area: 38.8?2
methyl methoxy(methyl)carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | M355728-250mg |
methyl methoxy(methyl)carbamate |
153654-07-0 | 250mg |
$ 70.00 | 2022-06-03 | ||
| TRC | M355728-500mg |
methyl methoxy(methyl)carbamate |
153654-07-0 | 500mg |
$ 95.00 | 2022-06-03 | ||
| TRC | M355728-2.5g |
methyl methoxy(methyl)carbamate |
153654-07-0 | 2.5g |
$ 365.00 | 2022-06-03 | ||
| Chemenu | CM535247-250mg |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95%+ | 250mg |
$75 | 2023-02-02 | |
| Chemenu | CM535247-1g |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95%+ | 1g |
$150 | 2023-02-02 | |
| Chemenu | CM535247-5g |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95%+ | 5g |
$456 | 2023-02-02 | |
| Chemenu | CM535247-10g |
Methyl methoxy(methyl)carbamate |
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| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1051549-100mg |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95% | 100mg |
¥379 | 2023-04-15 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1051549-250mg |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95% | 250mg |
¥681 | 2023-04-15 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1051549-1g |
Methyl methoxy(methyl)carbamate |
153654-07-0 | 95% | 1g |
¥1264 | 2023-04-15 |
methyl methoxy(methyl)carbamate Suppliers
methyl methoxy(methyl)carbamate Related Literature
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
Additional information on methyl methoxy(methyl)carbamate
Introduction to Methyl Methoxy(Methyl)Carbamate (CAS No. 153654-07-0)
Methyl methoxy(methyl)carbamate, a compound with the chemical formula C?H??NO?, is a derivative of carbamate that has garnered significant attention in the field of pharmaceutical and agrochemical research. This compound is identified by its unique CAS number, CAS No. 153654-07-0, which distinguishes it from other related molecules. The structural features of methyl methoxy(methyl)carbamate, particularly its methyl and methoxy substituents, contribute to its versatile reactivity and potential applications in synthetic chemistry.
The carbamate functional group in methyl methoxy(methyl)carbamate plays a crucial role in its chemical behavior. Carbamates are known for their ability to act as intermediates in the synthesis of various biologically active compounds. The presence of both methyl and methoxy groups enhances the compound's solubility and reactivity, making it a valuable building block in organic synthesis. Recent studies have highlighted the compound's potential in the development of novel agrochemicals and pharmaceuticals.
In the realm of pharmaceutical research, methyl methoxy(methyl)carbamate has been explored for its potential as a precursor in the synthesis of active pharmaceutical ingredients (APIs). The compound's structural flexibility allows for modifications that can tailor its biological activity. For instance, researchers have investigated its use in the development of pesticides and herbicides, where its carbamate moiety contributes to its efficacy against various pests and weeds.
The agrochemical applications of methyl methoxy(methyl)carbamate are particularly noteworthy. Its ability to interact with biological targets at low concentrations makes it an attractive candidate for environmentally friendly pest control solutions. Furthermore, the compound's stability under various environmental conditions enhances its practicality in field applications. Recent advancements in green chemistry have prompted researchers to explore sustainable methods for synthesizing this compound, reducing the environmental impact of its production.
From a synthetic chemistry perspective, methyl methoxy(methyl)carbamate serves as a versatile intermediate. Its reactivity allows for the introduction of additional functional groups, enabling the creation of complex molecules with tailored properties. This has led to its use in the synthesis of pharmaceutical intermediates, including those involved in the treatment of neurological disorders and infectious diseases. The compound's ability to undergo various chemical transformations makes it a valuable tool in medicinal chemistry.
The pharmacological potential of methyl methoxy(methyl)carbamate has been further explored through computational modeling and experimental studies. These investigations have revealed that the compound exhibits promising activity against certain enzymes and receptors implicated in human diseases. For example, studies suggest that derivatives of this compound may inhibit enzymes involved in inflammation and pain signaling, making them potential candidates for therapeutic development.
In conclusion, methyl methoxy(methyl)carbamate (CAS No. 153654-07-0) is a multifaceted compound with significant applications in pharmaceuticals and agrochemicals. Its unique structural features, including the presence of methyl and methoxy groups, contribute to its versatility as a synthetic intermediate. The compound's potential as a precursor for APIs and its role in developing environmentally friendly pest control solutions underscore its importance in modern chemistry research.
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