Cas no 1343983-86-7 (Methyl 1-cyano-3-methylcyclobutane-1-carboxylate)
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate Chemical and Physical Properties
Names and Identifiers
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- methyl 1-cyano-3-methylcyclobutane-1-carboxylate
- NE48678
- Methyl 1-cyano-3-methylcyclobutane-1-carboxylate
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- Inchi: 1S/C8H11NO2/c1-6-3-8(4-6,5-9)7(10)11-2/h6H,3-4H2,1-2H3
- InChI Key: KKVFPNSVHBFTBY-UHFFFAOYSA-N
- SMILES: O(C)C(C1(C#N)CC(C)C1)=O
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 220
- Topological Polar Surface Area: 50.1
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Warning Statement: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B496833-10mg |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 10mg |
$ 70.00 | 2022-06-07 | ||
| TRC | B496833-50mg |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 50mg |
$ 210.00 | 2022-06-07 | ||
| TRC | B496833-100mg |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 100mg |
$ 340.00 | 2022-06-07 | ||
| Chemenu | CM464638-250mg |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95%+ | 250mg |
$469 | 2022-12-31 | |
| Chemenu | CM464638-500mg |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95%+ | 500mg |
$744 | 2022-12-31 | |
| Chemenu | CM464638-1g |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95%+ | 1g |
$948 | 2022-12-31 | |
| Enamine | EN300-106323-0.05g |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95% | 0.05g |
$202.0 | 2023-10-28 | |
| Enamine | EN300-106323-0.1g |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95% | 0.1g |
$301.0 | 2023-10-28 | |
| Enamine | EN300-106323-0.25g |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95% | 0.25g |
$431.0 | 2023-10-28 | |
| Enamine | EN300-106323-0.5g |
methyl 1-cyano-3-methylcyclobutane-1-carboxylate |
1343983-86-7 | 95% | 0.5g |
$679.0 | 2023-10-28 |
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate Suppliers
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate Related Literature
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Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
Additional information on Methyl 1-cyano-3-methylcyclobutane-1-carboxylate
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate (CAS No. 1343983-86-7): An Overview
Methyl 1-cyano-3-methylcyclobutane-1-carboxylate (CAS No. 1343983-86-7) is a synthetic compound that has garnered significant attention in the fields of organic chemistry and pharmaceutical research. This compound, characterized by its unique cyclobutane ring and cyano group, exhibits a range of interesting properties that make it a valuable intermediate in the synthesis of various bioactive molecules and pharmaceuticals.
The chemical structure of Methyl 1-cyano-3-methylcyclobutane-1-carboxylate consists of a cyclobutane ring with a methyl group and a cyano group attached to the same carbon atom, along with a carboxylate ester group. This arrangement imparts specific reactivity and stability characteristics, making it an attractive candidate for various chemical transformations.
Recent studies have highlighted the potential applications of Methyl 1-cyano-3-methylcyclobutane-1-carboxylate in the development of new drugs. For instance, its use as a building block in the synthesis of antiviral agents has been explored. The cyano group can be readily converted into other functional groups, such as amides or amines, which are crucial for the biological activity of many pharmaceuticals.
In addition to its role in drug synthesis, Methyl 1-cyano-3-methylcyclobutane-1-carboxylate has also been investigated for its potential in materials science. The rigid cyclobutane ring and the presence of the cyano group can contribute to the formation of polymers with unique mechanical and thermal properties. These properties make it a promising candidate for applications in advanced materials and coatings.
The synthesis of Methyl 1-cyano-3-methylcyclobutane-1-carboxylate typically involves multi-step processes that require precise control over reaction conditions. One common approach is to start with a cyclobutane derivative and introduce the cyano and carboxylate groups through selective functionalization reactions. The choice of reagents and catalysts plays a crucial role in achieving high yields and purity.
From a safety perspective, handling Methyl 1-cyano-3-methylcyclobutane-1-carboxylate requires adherence to standard laboratory practices to ensure the well-being of researchers and the integrity of experimental results. Proper storage conditions, such as maintaining dryness and avoiding exposure to high temperatures, are essential to preserve its stability.
In conclusion, Methyl 1-cyano-3-methylcyclobutane-1-carboxylate (CAS No. 1343983-86-7) is a versatile compound with significant potential in both pharmaceutical research and materials science. Its unique chemical structure and reactivity make it an important intermediate in the synthesis of bioactive molecules and advanced materials. Ongoing research continues to uncover new applications and optimizations for this compound, further solidifying its importance in the scientific community.
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