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124621

Sigma-Aldrich

Methyl 5-bromosalicylate

95%

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About This Item

Linear Formula:
BrC6H3-2-(OH)CO2CH3
CAS Number:
4068-76-2
Molecular Weight:
231.04
EC Number:
223-776-4
MDL number:
MFCD00016460
UNSPSC Code:
12352100
PubChem Substance ID:
24847620
NACRES:
NA.22

Assay

95%

form

solid

mp

61-65 °C (lit.)

functional group

bromo

SMILES string

COC(=O)c1cc(Br)ccc1O

InChI

1S/C8H7BrO3/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4,10H,1H3

InChI key

FJYDBKPPGRZSOZ-UHFFFAOYSA-N

Related Categories

Application

Methyl 5-bromosalicylate was used as starting reagent in the synthesis of immobilization precursor of photoswitchable piperidine base.

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
BCBT9479
BCBD1669V
BCBR6428V
BCBS1319V
BCBJ1509V

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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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