- Benzamides of pyrazolyl-amino-pyrimidinyl derivatives, and compositions and methods thereof, World Intellectual Property Organization, , ,
Cas no 97421-23-3 (1-cyclohexyl-1H-pyrazol-4-amine)
97421-23-3 structure
Product Name:1-cyclohexyl-1H-pyrazol-4-amine
CAS No:97421-23-3
MF:C9H15N3
MW:165.235501527786
MDL:MFCD09965617
CID:1002165
Update Time:2025-09-27
1-cyclohexyl-1H-pyrazol-4-amine Chemical and Physical Properties
Names and Identifiers
-
- 1-cyclohexyl-1H-pyrazol-4-amine
- 1-cyclohexylpyrazol-4-amine
- 1-Cyclohexyl-1H-pyrazol-4-amine (ACI)
- 4-Amino-1-cyclohexylpyrazole
-
- MDL： MFCD09965617
- Inchi： 1S/C9H15N3/c10-8-6-11-12(7-8)9-4-2-1-3-5-9/h6-7,9H,1-5,10H2
- InChI Key： PJWCERWSFRWQNV-UHFFFAOYSA-N
- SMILES： N1N(C2CCCCC2)C=C(N)C=1
Computed Properties
- Exact Mass: 165.126597491 g/mol
- Monoisotopic Mass: 165.126597491 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 143
- 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
- Molecular Weight: 165.24
- XLogP3: 1.3
- Topological Polar Surface Area: 43.8?2
1-cyclohexyl-1H-pyrazol-4-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 064910-1g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 97% | 1g |
￡143.00 | 2022-03-01 | |
| Fluorochem | 064910-5g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 97% | 5g |
￡518.00 | 2022-03-01 | |
| Fluorochem | 064910-10g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 97% | 10g |
￡960.00 | 2022-03-01 | |
| Chemenu | CM316222-5g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 95%+ | 5g |
$937 | 2024-07-18 | |
| Apollo Scientific | OR110923-1g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 1g |
￡138.00 | 2023-09-02 | ||
| Apollo Scientific | OR110923-5g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 5g |
￡501.00 | 2023-09-02 | ||
| abcr | AB419175-1 g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 1g |
€212.70 | 2022-03-02 | ||
| abcr | AB419175-5 g |
1-Cyclohexyl-1H-pyrazol-4-amine |
97421-23-3 | 5g |
€627.70 | 2022-03-02 | ||
| Alichem | A049006103-250mg |
1-Cyclohexyl-1h-pyrazol-4-amine |
97421-23-3 | 95% | 250mg |
$257.40 | 2023-08-31 | |
| Alichem | A049006103-1g |
1-Cyclohexyl-1h-pyrazol-4-amine |
97421-23-3 | 95% | 1g |
$614.25 | 2023-08-31 |
1-cyclohexyl-1H-pyrazol-4-amine Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Iron , Ammonium chloride Solvents: Ethanol , Water ; 3 h, 85 °C
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ; overnight, rt
Reference
- Preparation of 1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidine-3-one derivatives as WEE-1 kinase inhibitors for the treatment of cancers, World Intellectual Property Organization, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Ethanol ; 8 h, rt
Reference
- Pyrrolopyrimidine compound, its preparation method and application in preparing drug for preventing and treating Wee1 protein kinase related disease, China, , ,
Production Method 4
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ; overnight, rt
Reference
- Pyrrolo[3,2-d]pyrimidine derivatives as IRAK4 inhibitors and their preparation, pharmaceutical compositions and use in the treatment of mammal diseases, World Intellectual Property Organization, , ,
Production Method 5
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ; 16 h, 50 °C
1.2 Reagents: Hydrogen Catalysts: Nickel Solvents: Ethanol , Ethyl acetate ; 5 h, rt
1.2 Reagents: Hydrogen Catalysts: Nickel Solvents: Ethanol , Ethyl acetate ; 5 h, rt
Reference
- Preparation of pyrazole derivatives as JAK inhibitors for treatment of autoimmune disease or cancer, World Intellectual Property Organization, , ,
Production Method 6
Reaction Conditions
Reference
- Herbicide containing metribuzin in combination with 1,4-disubstituted pyrazole derivatives, Federal Republic of Germany, , ,
1-cyclohexyl-1H-pyrazol-4-amine Raw materials
1-cyclohexyl-1H-pyrazol-4-amine Preparation Products
1-cyclohexyl-1H-pyrazol-4-amine Related Literature
-
Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
-
Martin R. Ward,Gary W. Copeland,Andrew J. Alexander Chem. Commun., 2010,46, 7634-7636
-
Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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