B7252
1-Bromo-2-naphthoic acid
≥98%
Synonym(s):
1-Bromo-2-naphthalenecarboxylic acid
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About This Item
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Assay
≥98%
form
powder
SMILES string
OC(=O)c1ccc2ccccc2c1Br
InChI
1S/C11H7BrO2/c12-10-8-4-2-1-3-7(8)5-6-9(10)11(13)14/h1-6H,(H,13,14)
InChI key
VUVIRKAVBZITDO-UHFFFAOYSA-N
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Application
Reactant involved in synthesis of:
- Binaphthyl-based amino acids and amino alcohols via domino coupling reactions and lactam ring opening of intermediates
- Benzimidazoles and benzimidazolequinone derivatives via cyclocondensation
- Axially chiral biaryls via Suzuki-Miyaura reactions
- Aryl ring-fused benzimidazolequinones via radical cyclization
- Probes for human cytochrome P450 enzymes
- Phananthridinone derivatives via domino coupling reactions
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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