| Identification | More | [Name]
1-BROMO-2-NAPHTHOIC ACID | [CAS]
20717-79-7 | [Synonyms]
1,2-BNCA
Einecs 243-984-9
RARECHEM AL BE 0298
1-BroMo-2-phthoic acid
1-BROMO-2-NAPTHOIC ACID
1-Bromo-2-naphtoic acid
1-BROMO-2-NAPHTHOIC ACID
1-Bromo-2-naphthoic Acid >
1-bromonaphthalene-2-carboxylicaci
1-BROMO-2-NAPHTHALENECARBOXYLIC ACID
1-Bromonaphthalene-2-carboxylic acid
1-bromo-2-naphthoic acid crystalline
2-Naphthalenecarboxylicacid, 1-bromo- | [EINECS(EC#)]
243-984-9 | [Molecular Formula]
C11H7BrO2 | [MDL Number]
MFCD00021408 | [Molecular Weight]
251.08 | [MOL File]
20717-79-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
191 °C | [Boiling point ]
372.7±25.0 °C(Predicted) | [density ]
1.648 | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Powder or Crystalline Powder | [pka]
2.85±0.30(Predicted) | [color ]
White to yellow to light brown | [InChIKey]
VUVIRKAVBZITDO-UHFFFAOYSA-N | [CAS DataBase Reference]
20717-79-7(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
Solid | [Uses]
1-Bromo-2-naphthoic acid is a 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.
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