159549
4-(Bromomethyl)benzoic acid
97%
Synonym(s):
α-Bromo-p-toluic acid
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About This Item
Linear Formula:
BrCH2C6H4CO2H
CAS Number:
Molecular Weight:
215.04
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-343-3
Beilstein/REAXYS Number:
1862870
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
mp
224-229 °C (lit.)
functional group
bromo, carboxylic acid
SMILES string
OC(=O)c1ccc(CBr)cc1
InChI
1S/C8H7BrO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5H2,(H,10,11)
InChI key
CQQSQBRPAJSTFB-UHFFFAOYSA-N
Application
4-(Bromomethyl)benzoic acid was used in the chemical modification of 5,10,15,20-tetra(m-hydroxyphenyl)chlorin (temoporfin), second generation photosensitizer. It was also used in the synthesis of 4-(5-arylidene-2,4-dioxothiazolidin-3-yl) methylbenzoic acids.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Chendong Ji et al.
Chemistry, an Asian journal, 11(16), 2316-2321 (2016-07-14)
Electrospun ultrathin fiber-based sensors are desirable because of their practicality and sensitivity. Ammonia-detection systems are in high demand in different areas, including the industrial and agricultural fields. However, current technologies rely on large and complex instruments that restrict their actual
Rosanna Maccari et al.
Bioorganic & medicinal chemistry, 15(15), 5137-5149 (2007-06-05)
4-(5-Arylidene-2,4-dioxothiazolidin-3-yl)methylbenzoic acids (2) were synthesized and evaluated in vitro as inhibitors of PTP1B and LMW-PTP, two protein tyrosine phosphatases (PTPs) which act as negative regulators of the metabolic and mitotic signalling of insulin. The synthesis of compounds 2 represents an
Marcela S Lopes et al.
European journal of medicinal chemistry, 46(11), 5443-5447 (2011-09-24)
A series of nitroaromatic compounds was synthesized and evaluated as potential antileishmanial and trypanocidal agents. Five compounds exerted significant anti-leishmanial activity in vitro against promastigotes forms of Leishmania (L.) amazonensis, with IC(50) in the range of 23-59 μmol L(-1), but
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 159549-5G | 04061838744654 |
| 159549-10G | 04061838744647 |
| 159549-50G | 04061832489285 |