1,3-dimethyl-1H-pyrazol-4-amine hydrochloride

Base Information

• Chemical Name: 1,3-dimethyl-1H-pyrazol-4-amine hydrochloride
• CAS No.: 1147222-02-3
• Molecular Formula: C₅H₉N₃*2ClH
• Molecular Weight: 184.068
• Hs Code.: 2933199090
• European Community (EC) Number: 802-458-4
• DSSTox Substance ID: DTXSID10506902
• Mol file: 1147222-02-3.mol

Synonyms:1,3-dimethyl-1H-pyrazol-4-amine hydrochloride;1147222-02-3;1,3-dimethylpyrazol-4-amine;hydrochloride;1,3-DIMETHYL-1H-PYRAZOL-4-AMINE HCL;4-Amino-1,3-dimethyl-1H-pyrazole hydrochloride;1,3-DIMETHYL-1H-PYRAZOL-4-YLAMINE HYDROCHLORIDE;1,3-dimethylpyrazol-4-amine hydrochloride;SCHEMBL1557971;DTXSID10506902;ZDOGXPGAEYKUJK-UHFFFAOYSA-N;XVB22202;CL3439;MFCD02253769;AKOS004107406;AB89890;PS-8933;4-Amino-1,3-dimethyl-1H-pyrazole HCl;AM802955;1,3-dimethyl-pyrazol-4-amine hydrochloride;CS-0141734;1,3-dimethyl-1H-pyrazol-4-aminehydrochloride;EN300-155587;A894148;Z1742055027;1,3-Dimethyl-1H-pyrazol-4-amine--hydrogen chloride (1/1);1H-Pyrazol-4-amine, 1,3-dimethyl-, hydrochloride (1:1)

Chemical Property of 1,3-dimethyl-1H-pyrazol-4-amine hydrochloride

Chemical Property:

• PSA: 43.84000
• LogP: 1.69390
• Storage Temp.: Sealed in dry,Room Temperature
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 147.0563250
• Heavy Atom Count: 9
• Complexity: 83.7

Purity/Quality:

97% ^*data from raw suppliers

1,3-Dimethyl-1H-pyrazol-4-amineHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=NN(C=C1N)C.Cl

Technology Process of 1,3-dimethyl-1H-pyrazol-4-amine hydrochloride

There total 1 articles about 1,3-dimethyl-1H-pyrazol-4-amine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

1,3-dimethyl-4-nitropyrazole → 1,3-dimethyl-1H-pyrazol-4-amine dihydrochloride (1147222-02-3,197367-87-6)

Guidance literature:

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In methanol; water; at 50 ℃; under 6205.94 Torr;

DOI:10.1021/op900296p

Reference yield: 90.0%

1,3-dimethyl-1H-pyrazol-4-amine dihydrochloride (1147222-02-3,197367-87-6) + (1R,2R)-2-(4-bromobenzoyl)cyclohexane-1-carboxylic acid (212757-09-0) → (1R,2R)-2-(4-bromobenzoyl)-N-(1,3-dimethyl-1H-pyrazol-4-yl)cyclohexane-1-carboxamide

Guidance literature:

With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; N-ethyl-N,N-diisopropylamine; In ethyl acetate; at 45 - 60 ℃;

DOI:10.1021/acs.jmedchem.8b02012

Reference yield: 84.0%

1,3-dimethyl-1H-pyrazol-4-amine dihydrochloride (1147222-02-3,197367-87-6) + 1,1'-Thiocarbonyldiimidazole (6160-65-2) → 4-isothiocyanato-1,3-dimethylpyrazole (1001500-07-7)

Guidance literature:

In 1,2-dichloro-ethane; at 20 ℃; for 5.5h; Inert atmosphere;

Downstream raw materials:

4-isothiocyanato-1,3-dimethylpyrazole

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