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190772

Sigma-Aldrich

4-Bromobenzamide

97%

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About This Item

Linear Formula:
BrC6H4CONH2
CAS Number:
698-67-9
Molecular Weight:
200.03
EC Number:
211-817-9
MDL number:
MFCD00007991
UNSPSC Code:
12352100
PubChem Substance ID:
24851460
NACRES:
NA.22

Assay

97%

form

powder

mp

190-193 °C (lit.)

functional group

amide

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBJ7064
STBD5831V
SHBB2095V
26196DM
17621AJ

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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
Electrochemical fluorination of aromatic compounds in anhydrous HF.
Shainyan BA and Danilevich YS.
Russ. J. Org. Chem., 42(2), 214-219 (2006)

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