Cas no 1079-46-5 (Methyl 5-chloro-1H-indazole-3-carboxylate)
Methyl 5-chloro-1H-indazole-3-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- Methyl 5-chloro-1H-indazole-3-carboxylate
- 5-Chloro-1H-indazole-3-carboxylic acid methyl ester
- 5-Chlor-3-methoxycarbonyl-indazol
- 5-chloro-1(2)H-indazole-3-carboxylic acid methyl ester
- methyl 5-chloroindazole-3-carboxylate
- QC-9440
- OFHGAYNAKIWVOL-UHFFFAOYSA-N
- 1611AA
- SB16354
- TRA0169736
- SY020632
- EN001929
- ST24047983
- 079M465
- 1H-Indazole-3-carboxylicacid, 5-chloro-, methyl ester
- Z2045464259
- SCHEMBL4793264
- AC-28250
- MFCD07371574
- CS-11431
- 1079-46-5
- C9H7ClN2O2
- AMY10358
- AKOS016009788
- CS-0085354
- FT-0751508
- Z1269190825
- 5-Chloro-2h-indazole-3-carboxylic acid methyl ester
- Y10018
- A895378
- DTXSID20506973
- G11405
- DB-059669
- METHYL5-CHLORO-1H-INDAZOLE-3-CARBOXYLATE
-
- MDL: MFCD07371574
- Inchi: 1S/C9H7ClN2O2/c1-14-9(13)8-6-4-5(10)2-3-7(6)11-12-8/h2-4H,1H3,(H,11,12)
- InChI Key: OFHGAYNAKIWVOL-UHFFFAOYSA-N
- SMILES: ClC1C=CC2=C(C=1)C(C(=O)OC)=NN2
Computed Properties
- Exact Mass: 210.02000
- Monoisotopic Mass: 210.0196052g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 237
- 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
- Surface Charge: 0
- Tautomer Count: 4
- XLogP3: 2.4
- Topological Polar Surface Area: 55
Experimental Properties
- Density: 1.453
- Boiling Point: 378.737 ℃ at 760 mmHg
- Flash Point: 182.854°C
- Refractive Index: 1.657
- PSA: 54.98000
- LogP: 2.00290
Methyl 5-chloro-1H-indazole-3-carboxylate Customs Data
- HS CODE:2933990090
- Customs Data:
China Customs Code:
2933990090Overview:
2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Methyl 5-chloro-1H-indazole-3-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A269001950-5g |
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| TRC | B495153-100mg |
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$ 135.00 | 2022-06-07 | ||
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD26942-250mg |
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1079-46-5 | 95% | 250mg |
¥257.0 | 2022-03-01 | |
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD26942-1g |
Methyl 5-chloro-1H-indazole-3-carboxylate |
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¥628.0 | 2022-03-01 | |
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD26942-5g |
Methyl 5-chloro-1H-indazole-3-carboxylate |
1079-46-5 | 95% | 5g |
¥2194.0 | 2022-03-01 | |
| Chemenu | CM150401-5g |
5-Chloro-1H-indazole-3-carboxylic acid methyl ester |
1079-46-5 | 97% | 5g |
$800 | 2021-08-05 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 45R0177-1g |
Methyl 5-chloro-1H-indazole-3-carboxylate |
1079-46-5 | 97% | 1g |
1679.12CNY | 2021-05-08 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 45R0177-5g |
Methyl 5-chloro-1H-indazole-3-carboxylate |
1079-46-5 | 97% | 5g |
6767.38CNY | 2021-05-08 |
Methyl 5-chloro-1H-indazole-3-carboxylate Related Literature
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Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023
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M. A. Piechowiak,A. Videcoq,R. Ferrando,D. Bochicchio,C. Pagnoux,F. Rossignol Phys. Chem. Chem. Phys., 2012,14, 1431-1439
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
Additional information on Methyl 5-chloro-1H-indazole-3-carboxylate
Recent Advances in the Research of Methyl 5-chloro-1H-indazole-3-carboxylate (CAS: 1079-46-5)
Methyl 5-chloro-1H-indazole-3-carboxylate (CAS: 1079-46-5) is a key intermediate in the synthesis of various biologically active compounds, particularly in the pharmaceutical and agrochemical industries. Recent studies have highlighted its significance in the development of novel therapeutic agents, owing to its versatile chemical structure and reactivity. This research brief aims to provide an overview of the latest advancements related to this compound, focusing on its synthesis, applications, and potential in drug discovery.
Recent literature has emphasized the role of Methyl 5-chloro-1H-indazole-3-carboxylate as a precursor in the synthesis of indazole-based derivatives, which exhibit a wide range of pharmacological activities. For instance, a study published in the Journal of Medicinal Chemistry (2023) demonstrated its utility in the development of kinase inhibitors, which are crucial for targeting cancer-related pathways. The compound's chloro and ester functional groups allow for further modifications, enabling the creation of diverse molecular scaffolds with enhanced bioactivity.
In addition to its pharmaceutical applications, Methyl 5-chloro-1H-indazole-3-carboxylate has been investigated for its potential in agrochemical research. A recent report in the Journal of Agricultural and Food Chemistry (2024) highlighted its use in the synthesis of novel herbicides with improved efficacy and environmental safety profiles. The compound's stability and reactivity make it an attractive candidate for designing next-generation agrochemicals.
From a synthetic chemistry perspective, advancements in catalytic methods have streamlined the production of Methyl 5-chloro-1H-indazole-3-carboxylate. A study in Organic Letters (2023) introduced a palladium-catalyzed cross-coupling approach that significantly improved the yield and purity of the compound. This methodological innovation not only enhances the scalability of its production but also reduces the environmental impact associated with traditional synthetic routes.
Looking ahead, the potential of Methyl 5-chloro-1H-indazole-3-carboxylate in drug discovery and development remains promising. Ongoing research is exploring its incorporation into more complex molecular architectures, such as PROTACs (Proteolysis Targeting Chimeras), which represent a cutting-edge approach in targeted protein degradation. Furthermore, computational studies are being employed to predict its interactions with biological targets, thereby accelerating the identification of new therapeutic candidates.
In conclusion, Methyl 5-chloro-1H-indazole-3-carboxylate (CAS: 1079-46-5) continues to be a focal point in chemical and pharmaceutical research. Its versatility, coupled with recent synthetic and methodological advancements, underscores its importance in the development of innovative therapeutic and agrochemical solutions. Future studies are expected to further elucidate its potential and expand its applications in diverse scientific domains.
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