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![9-Borabicyclo[3.3.1]nonane solution 0.5 M in THF](/deepweb/assets/sigmaaldrich/product/structures/180/891/8b64e597-269d-4780-98b6-40889dfd06b9/640/8b64e597-269d-4780-98b6-40889dfd06b9.png)
![9-Borabicyclo[3.3.1]nonane dimer](/deepweb/assets/sigmaaldrich/product/structures/203/431/624973a6-aec1-4b23-b6c4-013285ac418c/640/624973a6-aec1-4b23-b6c4-013285ac418c.png)
Quality Level
분석
97%
형태
powder
mp
190-193 °C (lit.)
작용기
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
일반 설명
Electrochemical fluorination of 4-bromobenzamide in anhydrous HF has been investigated.
애플리케이션
4-Bromobenzamide was used in the preparation of (N-benzylpiperidin-4-yl)-4-tri-n-butylstannylbenzamide.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Electrochemical fluorination of aromatic compounds in anhydrous HF.
Shainyan BA and Danilevich YS.
Russ. J. Org. Chem., 42(2), 214-219 (2006)
C S John et al.
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
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