All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C7H7BN4O2
CAS Number:
Molecular Weight:
189.97
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥95%
form
solid
mp
148-152 °C
storage temp.
2-8°C
SMILES string
OB(O)c1ccccc1-c2nnn[nH]2
InChI
1S/C7H7BN4O2/c13-8(14)6-4-2-1-3-5(6)7-9-11-12-10-7/h1-4,13-14H,(H,9,10,11,12)
InChI key
GVRXWYFECKHTSJ-UHFFFAOYSA-N
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Related Categories
Application
2-(Tetrazol-5-yl)phenylboronic acid can be used as a reactant to prepare:
- Biaryltetrazole derivatives via Suzuki-Miyaura cross-coupling with aryl and heteroaryl halides via formation of C-C bond.
- 2-Aminobenzoxazole derivatives containing biphenyl tetrazole as potent human chemR23 inhibitors.
- o-Phenylenediamine possessing tetrazolyl derivatives as potent inhibitors of indoleamine 2,3-dioxygenase.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Find documentation for the products that you have recently purchased in the Document Library.
The discovery and optimization of a series of 2-aminobenzoxazole derivatives as ChemR23 inhibitors
Imaizumi T, et al.
Bioorganic & Medicinal Chemistry, 27(21), 115091-115091 (2019)
Development of a series of novel o-phenylenediamine-based indoleamine 2, 3-dioxygenase 1 (IDO1) inhibitors
Williams DK, et al.
Bioorganic & Medicinal Chemistry Letters, 28(4), 732-736 (2018)
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