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tert-butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate

This protected pyrazole derivative contains both heterocyclic and tert-butyl ester functionalities supporting controlled reactivity. Researchers use it to explore heterocycle incorporation into peptides and ligand scaffolds. Its electronic profile aids mechanistic studies and structural modeling.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
tert-butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate(CAS 578008-32-9)

CAT No: R2105

CAS No:578008-32-9

Synonyms/Alias:578008-32-9;tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate;3-Amino-1-Boc-5-methyl-1H-pyrazole;1H-Pyrazole-1-carboxylicacid,3-amino-5-methyl-,1,1-dimethylethylester;MFCD13252375;tert-butyl 3-amino-5-methylpyrazole-1-carboxylate;SCHEMBL161429;GJDCNROAKOCYIQ-UHFFFAOYSA-N;1-boc-3-amino-5-methyl-pyrazole;DYA00832;1-Boc-3-amino-5-methyl-1H-pyrazole;AKOS024258768;AKOS037647138;AS-72542;SY060940;DB-315097;CS-0036055;W12764;EN300-7364853;tert-Butyl3-amino-5-methyl-1H-pyrazole-1-carboxylate;Z1216817739;3-Amino-5-methylpyrazole-1-carboxylic acid tert-butyl ester;1,1-Dimethylethyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate;3-Amino-5-methyl-pyrazole-1-carboxylic acid tert-butyl ester;tert-butyl 3-imino-5-methyl-2,3-dihydro-1H-pyrazole-1-carboxylate;887-631-2;

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M.F/Formula
C9H15N3O2
M.W/Mr.
197.23
InChI
InChI=1S/C9H15N3O2/c1-6-5-7(10)11-12(6)8(13)14-9(2,3)4/h5H,1-4H3,(H2,10,11)
InChI Key
GJDCNROAKOCYIQ-UHFFFAOYSA-N

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