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1-tert-butyl 2-methyl (2S,3R)-3-hydroxypyrrolidine-1,2-dicarboxylate

1-tert-butyl 2-methyl (2S,3R)-3-hydroxypyrrolidine-1,2-dicarboxylate

(3-methyl-1H-indazol-7-yl)boronic acid

(3-methyl-1H-indazol-7-yl)boronic acid

2,3-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole

$295.00
CAS No.: 1310383-43-7
Catalog No.: 171181
Purity: 95%
MF: C15H21BN2O2
MW: 272.157
Storage: 2-8 degree Celsius
SMILES: CN1N=C2C=CC=C(B3OC(C)(C)C(C)(C)O3)C2=C1C
For R&D use only. Not for human or animal use.
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171181
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5-bromo-2,3-dimethyl-2H-indazole
5-bromo-2,3-dimethyl-2H-indazole
1-[2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazol-4-yl]-1,3-diazinane-2,4-dione
1-[2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazol-4-yl]-1,3-diazinane-2,4-dione
1-[2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
1-[2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-4-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-4-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-5-yl]-1,3-diazinane-2,4-dione
1-[2-(2-aminoethyl)-2H-indazol-5-yl]-1,3-diazinane-2,4-dione
1-[2-(2-hydroxyethyl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
1-[2-(2-hydroxyethyl)-2H-indazol-6-yl]-1,3-diazinane-2,4-dione
2,3-dimethyl-2H-indazol-6-amine
2,3-dimethyl-2H-indazol-6-amine
2-methyl-3-(prop-1-en-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
2-methyl-3-(prop-1-en-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
5-bromo-2-methyl-2H-indazole-3-carbaldehyde
5-bromo-2-methyl-2H-indazole-3-carbaldehyde
2,3-dimethyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole; CAS No.: 1310383-43-7; This 2,3-dimethyl-4-boronic indazole derivative serves as building blocks for BTK inhibitor development. The dimethyl groups block metabolic hotspots while the boronic acid enables PROTAC conjugation. Our custom chemical synthesis companies employ cryogenic lithiation-borylation to achieve regioselective functionalization of sensitive indazoles.

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