173681
Methyl 4-methoxysalicylate
98%
Synonym(s):
Methyl 2-hydroxy-4-methoxybenzoate
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About This Item
Linear Formula:
CH3OC6H3(OH)CO2CH3
CAS Number:
Molecular Weight:
182.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-657-5
MDL number:
Assay:
98%
Form:
solid
InChI key
ZICRWXFGZCVTBZ-UHFFFAOYSA-N
InChI
1S/C9H10O4/c1-12-6-3-4-7(8(10)5-6)9(11)13-2/h3-5,10H,1-2H3
SMILES string
COC(=O)c1ccc(OC)cc1O
assay
98%
form
solid
mp
50-53 °C (lit.)
Application
Methyl 4-methoxysalicylate (methyl 2-hydroxy-4-methoxybenzoate) was used in the enantioselective synthesis of (+)-coriandrone A and B, two bioactive natural products.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Wenjing Wang et al.
Organic & biomolecular chemistry, 11(39), 6686-6690 (2013-08-30)
The first enantioselective total synthesis of (+)-coriandrone A and B, two bioactive natural products, has been achieved in 10 steps and 11 steps starting from commercially available methyl 2-hydroxy-4-methoxybenzoate. Key reactions include a Claison rearrangement, a Shi-type epoxidation-cyclization sequence and
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