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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

Quality Level

200

Assay

95%

form

solid

mp

61-65 °C (lit.)

functional group

bromo
ester

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

124621-5G:
124621-25G:
124621-BULK:
124621-VAR:

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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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