Cas no 1178433-11-8 (1-Pentyl-1H-pyrazol-3-amine)
1-Pentyl-1H-pyrazol-3-amine structure
Product Name:1-Pentyl-1H-pyrazol-3-amine
CAS No:1178433-11-8
MF:C8H15N3
MW:153.224801301956
MDL:MFCD12149359
CID:4683669
Update Time:2025-09-20
1-Pentyl-1H-pyrazol-3-amine Chemical and Physical Properties
Names and Identifiers
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- 1-Pentyl-1H-pyrazol-3-amine
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- MDL： MFCD12149359
- Inchi： 1S/C8H15N3/c1-2-3-4-6-11-7-5-8(9)10-11/h5,7H,2-4,6H2,1H3,(H2,9,10)
- InChI Key： ZIZHEYBVBRRMRQ-UHFFFAOYSA-N
- SMILES： N1(C=CC(N)=N1)CCCCC
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 4
- Complexity: 106
- Topological Polar Surface Area: 43.8
1-Pentyl-1H-pyrazol-3-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB422879-1 g |
1-Pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 1g |
€339.20 | 2022-03-02 | ||
| abcr | AB422879-5 g |
1-Pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 5g |
€765.20 | 2022-03-02 | ||
| Chemenu | CM331613-1g |
1-Pentyl-1h-pyrazol-3-amine |
1178433-11-8 | 95%+ | 1g |
$642 | 2023-02-03 | |
| Chemenu | CM331613-1g |
1-Pentyl-1h-pyrazol-3-amine |
1178433-11-8 | 95%+ | 1g |
$973 | 2021-08-18 | |
| Enamine | EN300-783485-0.05g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 0.05g |
$151.0 | 2025-02-22 | |
| Enamine | EN300-783485-0.1g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 0.1g |
$226.0 | 2025-02-22 | |
| Enamine | EN300-783485-0.25g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 0.25g |
$321.0 | 2025-02-22 | |
| Enamine | EN300-783485-0.5g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 0.5g |
$507.0 | 2025-02-22 | |
| Enamine | EN300-783485-1.0g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 1.0g |
$650.0 | 2025-02-22 | |
| Enamine | EN300-783485-2.5g |
1-pentyl-1H-pyrazol-3-amine |
1178433-11-8 | 95.0% | 2.5g |
$918.0 | 2025-02-22 |
1-Pentyl-1H-pyrazol-3-amine Related Literature
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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