124621
Methyl 5-bromosalicylate
95%
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About This Item
Linear Formula:
BrC6H3-2-(OH)CO2CH3
CAS Number:
Molecular Weight:
231.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-776-4
MDL number:
Assay:
95%
Form:
solid
InChI key
FJYDBKPPGRZSOZ-UHFFFAOYSA-N
InChI
1S/C8H7BrO3/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4,10H,1H3
SMILES string
COC(=O)c1cc(Br)ccc1O
assay
95%
form
solid
mp
61-65 °C (lit.)
functional group
bromo, ester
Quality Level
Related Categories
Application
Methyl 5-bromosalicylate was used as starting reagent in the synthesis of immobilization precursor of photoswitchable piperidine base.
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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Ragnar S Stoll et al.
Organic letters, 11(21), 4790-4793 (2009-10-02)
The synthesis of a photoswitchable piperidine base, carrying a monochlorosilane anchoring group, and its immobilization on silica gel, mimicking an oxide surface, is reported. Efficient photoswitching between the E and Z isomers of the azobenzene photochrome was demonstrated for the
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