Cas no 95853-51-3 (2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine)
2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine Chemical and Physical Properties
Names and Identifiers
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- 2-GIANIDINOTHIAZOLE-4-METHYLTHIOL
- 2-[4-(sulfanylmethyl)-1,3-thiazol-2-yl]guanidine
- Guanidine,[4-(mercaptomethyl)-2-thiazolyl]
- SCHEMBL8409815
- 2-[4-(Sulfanylmethyl)-1.3-thiazol-2-yl]guanidine
- 95853-51-3
- AKOS006304794
- Guanidine, [4-(mercaptomethyl)-2-thiazolyl]-
- DTXSID30539171
- N''-[4-(Sulfanylmethyl)-1,3-thiazol-2-yl]guanidine
- 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine
-
- Inchi: 1S/C5H8N4S2/c6-4(7)9-5-8-3(1-10)2-11-5/h2,10H,1H2,(H4,6,7,8,9)
- InChI Key: AHNNULCXEIGUHA-UHFFFAOYSA-N
- SMILES: S1C(/N=C(\N)/N)=NC(=C1)CS
Computed Properties
- Exact Mass: 188.01900
- Monoisotopic Mass: 188.01903862g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 157
- 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: -0.1
- Topological Polar Surface Area: 107?2
Experimental Properties
- PSA: 141.83000
- LogP: 1.75130
2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine Security Information
- Signal Word:warning
- Hazard Statement: H303+H313+H333
- 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)
2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | S689265-25mg |
2-[4-(Sulfanylmethyl)-1.3-thiazol-2-yl]guanidine |
95853-51-3 | 25mg |
$201.00 | 2023-05-17 | ||
| TRC | S689265-100mg |
2-[4-(Sulfanylmethyl)-1.3-thiazol-2-yl]guanidine |
95853-51-3 | 100mg |
$758.00 | 2023-05-17 | ||
| TRC | S689265-250mg |
2-[4-(Sulfanylmethyl)-1.3-thiazol-2-yl]guanidine |
95853-51-3 | 250mg |
$ 1200.00 | 2023-09-06 |
2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine Related Literature
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Abdelaziz Houmam,Emad M. Hamed Chem. Commun., 2012,48, 11328-11330
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Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
Additional information on 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine
Comprehensive Overview of 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine (CAS No. 95853-51-3): Properties, Applications, and Research Insights
The compound 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine (CAS No. 95853-51-3) is a specialized organic molecule that has garnered significant attention in pharmaceutical and biochemical research. Its unique structure, featuring a thiazole ring and a guanidine moiety, makes it a promising candidate for various applications, including drug development and material science. Researchers are particularly interested in its potential as a bioactive scaffold, given its ability to interact with biological targets such as enzymes and receptors.
In recent years, the demand for sulfur-containing heterocycles like 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine has surged due to their versatility in medicinal chemistry. The compound's sulfanylmethyl group enhances its reactivity, enabling it to participate in diverse chemical transformations. This property aligns with the growing trend of designing multifunctional ligands for targeted therapies, a hot topic in precision medicine. Scientists are also exploring its role in antioxidant and anti-inflammatory pathways, addressing common health concerns such as oxidative stress and chronic inflammation.
From a synthetic perspective, CAS No. 95853-51-3 is often discussed in the context of green chemistry and sustainable synthesis. Researchers are optimizing its production to minimize environmental impact, a priority for industries adhering to ESG (Environmental, Social, and Governance) principles. The compound's thiazole core is also a focal point for AI-driven drug discovery, as machine learning models increasingly predict its interactions with proteins, accelerating the development of novel therapeutics.
Beyond pharmaceuticals, 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine has potential applications in agrochemicals and material science. Its chelating properties make it useful in designing metal-organic frameworks (MOFs), which are pivotal in catalysis and gas storage. Additionally, its thiol group offers opportunities for surface modification in nanotechnology, a field gaining traction for innovations in wearable electronics and energy storage.
For researchers and industry professionals, understanding the structure-activity relationship (SAR) of 95853-51-3 is critical. Recent studies highlight its synergistic effects when combined with other bioactive molecules, a strategy employed in combination therapy for complex diseases. This aligns with the rising popularity of polypharmacology, where multi-target compounds are designed to enhance efficacy and reduce side effects.
In summary, 2-4-(Sulfanylmethyl)-1.3-thiazol-2-ylguanidine (CAS No. 95853-51-3) represents a multifaceted compound with broad scientific and industrial relevance. Its integration into cutting-edge research underscores its value in addressing contemporary challenges in healthcare, sustainability, and technology. As advancements in computational chemistry and high-throughput screening continue, this compound is poised to play an even greater role in innovation.
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