CAS 4023-02-3: 1H-Pyrazole-1-carboxamidine hydrochloride
Formula:C4H6N4·ClH
InChI:InChI=1S/C4H6N4.ClH/c5-4(6)8-3-1-2-7-8;/h1-3H,(H3,5,6);1H
InChI key:InChIKey=RBZRMBCLZMEYEH-UHFFFAOYSA-N
SMILES:C(=N)(N)N1C=CC=N1.Cl
Synonyms:- 1-Amidinopyrazole hydrochloride
- 1-Amidinopyrazole monohydrochloride
- 1H-Pyrazole-1-carboxamidine hydrochloride
- 1H-Pyrazole-1-carboxamidine monohydrochloride
- 1H-Pyrazole-1-carboxamidinehydrochloride
- 1H-Pyrazole-1-carboximidamide hydrochloride
- 1H-Pyrazole-1-carboximidamide, hydrochloride (1:1)
- 1H-Pyrazole-1-carboximidamide, monohydrochloride
- 1H-pyrazole-1-carboxamide hydrochloride (1:1)
- Praxadine hydrochloride
- Pyrazole-1-carboxamidine, hydrochloride
- See more synonyms
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Found 12 products.
Zanamivir impurity F CRS
CAS:Zanamivir impurity F CRSFormula:C6H5BrColor and Shape:Beige. Crystalline Powder., Beige. Crystalline Powder.Molecular weight:157.00791H-Pyrazole-1-carboxamidine monohydrochloride, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C4H6N4Purity:99%Color and Shape:White to light yellow, Crystalline powder or crystalsMolecular weight:110.121H-Pyrazole-1-Carboxamidine Hydrochloride
CAS:Formula:C4H7ClN4Purity:98%Color and Shape:SolidMolecular weight:146.578181-Amidinopyrazole Hydrochloride
CAS:Formula:C4H6N4·HClPurity:>98.0%(T)(HPLC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:146.581H-Pyrazole-1-carboxamidine hydrochloride, 99%
CAS:1H-Pyrazole-1-carboxamidine hydrochloride may be used in the following studies:Preparation of guanidylated hollow fiber membranes.SGuanylation of amines and in peptide synthesis.Synthesis of bis-guanidinium-cholesterol derivatives.This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C4H6N4Purity:99%Molecular weight:110.121H-Pyrazole-1-carboximidamide hydrochloride
CAS:Purity:97.0%Color and Shape:Solid, CrystallineMolecular weight:146.58000183105471(H)-Pyrazole-1-carboxamidine hydrochloride
CAS:Formula:C4H6N4HClPurity:≥ 98.0%Color and Shape:White to yellow crystalline powderMolecular weight:146.581H-Pyrazole-1-carboxamidine hydrochloride
CAS:1H-Pyrazole-1-carboxamidine hydrochloride is a potent inhibitor of the enzyme oleanolic acid cyclooxygenase. It has been shown to inhibit the growth of Cryptococcus neoformans in vitro, and also inhibits the production of hydrogen peroxide by neutrophils. 1H-Pyrazole-1-carboxamidine hydrochloride is a white solid with minimal toxicity in mice and rats. This compound has low solubility in water and is soluble in organic solvents such as ether, chloroform, or dichloromethane. 1H-Pyrazole-1-carboxamidine hydrochloride was synthesized using trifluoroacetic acid and amines to form the pyrazole ring during the reaction. 1H-Pyrazole-1-carboxamidine hydrochloride has been found to be stable under acidic conditions. The chelate ring in this molecule providesFormula:C4H7ClN4Purity:Min. 95%Color and Shape:White To Yellow SolidMolecular weight:146.58 g/mol1H-Pyrazole-1-carboxamidine hydrochloride
CAS:1H-Pyrazole-1-carboxamidine hydrochlorideFormula:C4H6N4·ClHPurity:By hplc: 99.6% by area (Typical Value in Batch COA)Color and Shape: white powderMolecular weight:146.58g/mol1H-Pyrazole-1-carboximidamide hydrochloride
CAS:1H-Pyrazole-1-carboximidamide hydrochloride, catalog number T67134 and CAS number 4023-02-3, is a valuable organic compound for life sciences research.Formula:C4H7ClN4Color and Shape:SolidMolecular weight:146.581H-Pyrazole-1-carboxamidine Hydrochloride
CAS:Controlled ProductApplications A stable and versatile reagent for the efficient and chemically specific guanylation of sterically unhindered primary and secondary aliphatic amines under mild conditions. Useful reagent in peptide synthesis. References Baslow, M., et al.: J. Inherit. Metab. Dis., 23, 684 (2000), Lee, Y., et al.: Bioorg. Med. Chem. Lett., 10, 2771 (2000), Baslow, M., et al.: Neurochem. Res., 27, 403 (2002),Formula:C4H6N4·ClHColor and Shape:NeatMolecular weight:146.58
