1H-Pyrazole-1-carboxamidine hydrochloride

1H-Pyrazole-1-carboxamidine hydrochloride Basic information
Product Name:1H-Pyrazole-1-carboxamidine hydrochloride
Synonyms:1H-PYRAZOLE-1-CARBOXAMIDINE HYDROCHLORIDE;1H-PYRAZOLE-1-CARBOXAMIDINE MONOHYDROCHLORIDE;1H-PYRAZOLE-1-CARBAMIDINE HCL;1-AMIDINOPYRAZOLE HYDROCHLORIDE;1-AMIDINOPYRAZOLE MONOHYDROCHLORIDE;PYRAZOLE CARBOXAMIDINE HCL;1H-Pyrazole-1-carboxaMidine Monohydrochloride, 99% 10GR;1H-Pyrazole-1-carboxaMidine Monohydrochloride, 99% 50GR
CAS:4023-02-3
MF:C4H7ClN4
MW:146.58
EINECS:429-520-1
Product Categories:amine;Heterocycles;Pyrazoles & Triazoles;Miscellaneous Reagents;Pyrazoles & Triazoles
Mol File:4023-02-3.mol
1H-Pyrazole-1-carboxamidine hydrochloride Structure
1H-Pyrazole-1-carboxamidine hydrochloride Chemical Properties
Melting point 167-170 °C(lit.)
storage temp. Inert atmosphere,Room Temperature
form Crystals or Crystalline Powder
color White to light yellow
Water Solubility Soluble
BRN 5448758
CAS DataBase Reference4023-02-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 36/37/38-36/37-34
Safety Statements 26-37/39-45-36/37/39
WGK Germany 3
10-21
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
1H-Pyrazole-1-carboxamidine hydrochloride Usage And Synthesis
Chemical Propertieswhite to light yellow crystals or crystalline
Uses1H-Pyrazole-1-carboxamidine hydrochloride may be used in the following studies: ? Preparation of guanidylated hollow fiber membranes. ? Guanylation of amines and in peptide synthesis. ? Synthesis of bis-guanidinium-cholesterol derivatives.
Uses1H-Pyrazole-1-carboxamidine hydrochloride is a stable and versatile reagent for the efficient and chemically specific guanylation of sterically unhindered primary and secondary aliphatic amines under mild conditions. 1H-Pyrazole-1-carboxamidine hydrochloride is a useful reagent in peptide synthesis
General Description1H-Pyrazole-1-carboxamidine hydrochloride, a pyrazole derivative, is a heterocyclic compound. It is widely used in drug syntheses studies. Pyrazole ring forms the main core of various nonsteroidal anti-inflammatory drugs (NSAIDs) and antihypertensive drugs.
1H-Pyrazole-1-carboxamidine hydrochloride Preparation Products And Raw materials
Preparation ProductsZANAMIVIR HYDRATE-->morpholine-4-carboximidamide-->{[AMINO(IMINO)METHYL]AMINO}ACETICACIDHYDROCHLORIDE-->Benzenesulfonamide, 4-[(aminoiminomethyl)amino]--->N-(4-METHOXYPHENYL)GUANIDINEHYDROCHLORIDE
1H-PYRAZOLE-1YL-N,N-DIMETHYLAMIDINE HYDROCHLORIDE 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one 2,3,3-TRICHLORO-1-[2-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)-4,5-DIHYDRO-1H-IMIDAZOL-1-YL]PROP-2-EN-1-ONE 5-CHLORO-4-([2-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)-4,5-DIHYDRO-1H-IMIDAZOL-1-YL]SULFONYL)-1,3-DIMETHYL-1H-PYRAZOLE Topotecan hydrochloride Pyraclostrobin N(sup 4)-(1,1-Dimethylethyl)-7-methylpyrazolo(1,5-a)-1,3,5-triazine-2, 4-diamine, hydrochloride N(sup 4)-2-Propenylpyrazolo(1,5-a)-1,3,5-triazine-2,4-diamine, hydroch loride hydrate (2:2:1) AKOS BBS-00002961 Zolpidem FORMAMIDINE HYDROCHLORIDE Pyrazole N''1-METHYL-1H-PYRAZOLE-1-CARBOXAMIDINE HYDROCHLORIDE Zolpidem tartrate 2,4-Diamino-pyrazolo(1,5-a)-s-triazine hydrochloride hemihydrate N(sup 4),7-Dimethylpyrazolo(1,5-a)-1,3,5-triazine-2,4-diamine, hydroch loride hydrate (2:2:1) 5-[3-(4-CHLOROPHENYL)-5-(TRIFLUOROMETHYL)-1H-PYRAZOL-1-YL]-7H-[1,2,4]TRIAZOLO[1,5-D][1,2,4]TRIAZEPIN-8(9H)-IMINE 1H-Pyrazole-1-carboxamidine hydrochloride

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