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Assay
97%
form
powder
mp
190-193 °C (lit.)
functional group
amide
bromo
SMILES string
NC(=O)c1ccc(Br)cc1
InChI
1S/C7H6BrNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)
InChI key
ZRWNRAJCPNLYAK-UHFFFAOYSA-N
Related Categories
General description
Electrochemical fluorination of 4-bromobenzamide in anhydrous HF has been investigated.
Application
4-Bromobenzamide was used in the preparation of (N-benzylpiperidin-4-yl)-4-tri-n-butylstannylbenzamide.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
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Cancer research, 55(14), 3022-3027 (1995-07-15)
The synthesis of [125I]-N-(N-benzylpiperidin-4-yl)-4-iodobenzamide (4-[125I]BP), a novel radiopharmaceutical that possesses high affinity for both sigma-1 and sigma-2 receptor subtypes, and its binding characteristics to MCF-7 breast cancer cells are described. To obtain high yields (with high specific activity) of radioiodinated
Electrochemical fluorination of aromatic compounds in anhydrous HF.
Russ. J. Org. Chem., 42(2), 214-219 (2006)
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