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Structure

1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester

CAS
864770-82-1
Catalog Number
ACM864770821
Category
Other Products
Molecular Weight
358.239680 [g/mol]
Molecular Formula
C19H27BN2O4

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Specification

Synonyms
864770-82-1, 1-N-BOC-3-METHYL-INDAZOLE-5-BORONIC ACID PINACOL ESTER, 1-N-Boc-3-Methylindazole-5-boronic acid pinacol ester, 1-BOC-3-METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDAZOLE, TERT-BUTYL 3-METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-INDAZOLE-1-CARBOXYLATE, SureCN2355889, AKOS015999146, MB13495, RL05342, AK-40747, KB-12995, A-9247, 1-N-BOC-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-3-METHYL-INDAZOLE, TERT-BUTYL 3-METHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-INDAZOLE-1-CARBOXYLATE
IUPAC Name
tert-butyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indazole-1-carboxylate
Canonical SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)N(N=C3C)C(=O)OC(C)(C)C
InChI Key
FQAORYQTZLGOBK-UHFFFAOYSA-N
Exact Mass
358.20600
H-Bond Acceptor
5
H-Bond Donor
0

Upstream Synthesis Route 1

  • 552331-49-4
  • 73183-34-3
  • 864770-82-1

Reference: [1] Patent: US2008/153813, 2008, A1, . Location in patent: Page/Page column 24

Upstream Synthesis Route 2

  • 552331-16-5
  • 864770-82-1

Reference: [1] Journal of Medicinal Chemistry, 2017, vol. 60, # 14, p. 6018 - 6035

Upstream Synthesis Route 3

  • 198477-89-3
  • 864770-82-1

Reference: [1] Journal of Medicinal Chemistry, 2017, vol. 60, # 14, p. 6018 - 6035

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