Cas no 762192-22-3 (1-methylcyclopropane-1-carboximidamide)
1-methylcyclopropane-1-carboximidamide Chemical and Physical Properties
Names and Identifiers
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- 1-Methylcyclopropanecarboxamidine
- Cyclopropanecarboximidamide, 1-methyl-
- 1-methylcyclopropane-1-carboximidamide
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- Inchi: 1S/C5H10N2/c1-5(2-3-5)4(6)7/h2-3H2,1H3,(H3,6,7)
- InChI Key: YVODAGKDGITUPJ-UHFFFAOYSA-N
- SMILES: NC(C1(C)CC1)=N
Computed Properties
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 7
- Rotatable Bond Count: 1
- Complexity: 103
- Topological Polar Surface Area: 49.9
1-methylcyclopropane-1-carboximidamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1829404-1g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 1g |
$1029.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-5g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 5g |
$2981.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-10g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 10g |
$4421.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-0.05g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 0.05g |
$864.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-0.1g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 0.1g |
$904.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-0.25g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 0.25g |
$946.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-0.5g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 0.5g |
$987.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-1.0g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 1g |
$1029.0 | 2023-06-03 | ||
| Enamine | EN300-1829404-2.5g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 2.5g |
$2014.0 | 2023-09-19 | ||
| Enamine | EN300-1829404-5.0g |
1-methylcyclopropane-1-carboximidamide |
762192-22-3 | 5g |
$2981.0 | 2023-06-03 |
1-methylcyclopropane-1-carboximidamide Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
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Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
Additional information on 1-methylcyclopropane-1-carboximidamide
Exploring the Chemistry and Applications of 1-Methylcyclopropane-1-carboximidamide (CAS No. 762192-22-3)
In the realm of organic chemistry, 1-methylcyclopropane-1-carboximidamide (CAS No. 762192-22-3) stands out as a fascinating compound with unique structural and functional properties. This molecule, characterized by its cyclopropane ring and carboximidamide functional group, has garnered attention for its potential applications in pharmaceuticals, agrochemicals, and material science. Researchers and industry professionals are increasingly interested in this compound due to its versatility and the growing demand for novel chemical entities in various fields.
The chemical structure of 1-methylcyclopropane-1-carboximidamide features a three-membered cyclopropane ring, which is known for its high ring strain and reactivity. The presence of the carboximidamide group (-C(=NH)NH2) further enhances its reactivity, making it a valuable intermediate in synthetic chemistry. The compound's molecular formula is C5H10N2, and its molecular weight is approximately 98.15 g/mol. These properties make it a subject of interest for researchers exploring new synthetic pathways and functional materials.
One of the most compelling aspects of 1-methylcyclopropane-1-carboximidamide is its potential role in drug discovery. The cyclopropane moiety is a common feature in many bioactive molecules, contributing to their stability and pharmacokinetic properties. For instance, cyclopropane-containing compounds have been used in the development of antiviral, antibacterial, and anticancer agents. The carboximidamide group, on the other hand, can participate in hydrogen bonding and other molecular interactions, which are crucial for drug-receptor binding. This dual functionality positions 1-methylcyclopropane-1-carboximidamide as a promising candidate for the design of new therapeutic agents.
Beyond pharmaceuticals, 1-methylcyclopropane-1-carboximidamide has potential applications in agrochemicals. The agricultural industry is constantly seeking innovative solutions to enhance crop protection and yield. Compounds with cyclopropane rings have been explored for their pesticidal and herbicidal activities. The reactivity of the carboximidamide group could also be harnessed to develop new classes of agrochemicals with improved efficacy and environmental safety. As sustainability becomes a key focus in agriculture, the demand for such advanced chemical solutions is expected to rise.
In material science, 1-methylcyclopropane-1-carboximidamide could play a role in the development of novel polymers and functional materials. The strained cyclopropane ring can impart unique mechanical and thermal properties to polymers, while the carboximidamide group can facilitate cross-linking and other chemical modifications. These characteristics make the compound a potential building block for high-performance materials used in coatings, adhesives, and composites. Researchers are particularly interested in exploring its use in smart materials that respond to environmental stimuli.
The synthesis of 1-methylcyclopropane-1-carboximidamide typically involves the reaction of 1-methylcyclopropanecarbonitrile with ammonia or a related nucleophile. This process highlights the compound's role as an intermediate in more complex synthetic routes. Advances in catalytic methods and green chemistry are expected to improve the efficiency and sustainability of its production. As the chemical industry moves toward greener practices, the development of eco-friendly synthesis methods for compounds like 1-methylcyclopropane-1-carboximidamide will be a key area of research.
Market trends indicate a growing interest in specialty chemicals, including 1-methylcyclopropane-1-carboximidamide. The compound's unique properties and potential applications align with the increasing demand for high-value chemical intermediates. Companies specializing in fine chemicals and custom synthesis are likely to see opportunities in supplying this compound to pharmaceutical, agrochemical, and material science sectors. Additionally, the rise of AI-driven drug discovery and computational chemistry tools is expected to accelerate the identification of new uses for such molecules, further driving market growth.
For researchers and industry professionals, understanding the safety and handling of 1-methylcyclopropane-1-carboximidamide is essential. While the compound is not classified as hazardous under standard regulations, proper laboratory practices should always be followed. This includes the use of personal protective equipment (PPE) and adherence to guidelines for chemical storage and disposal. As with any chemical, thorough risk assessment and safety protocols are necessary to ensure safe handling and use.
In conclusion, 1-methylcyclopropane-1-carboximidamide (CAS No. 762192-22-3) is a versatile and promising compound with applications spanning pharmaceuticals, agrochemicals, and material science. Its unique structural features, including the cyclopropane ring and carboximidamide group, make it a valuable intermediate and a subject of ongoing research. As the chemical industry continues to evolve, compounds like 1-methylcyclopropane-1-carboximidamide will play a critical role in driving innovation and addressing global challenges. Stay tuned for further developments in this exciting field of chemistry.
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