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About This Item
Linear Formula:
(CH3O)2C6H3CO2CH3
CAS Number:
Molecular Weight:
196.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
solid
bp
298 °C (lit.)
mp
42-43 °C (lit.)
functional group
ester
SMILES string
COC(=O)c1cc(OC)cc(OC)c1
InChI
1S/C10H12O4/c1-12-8-4-7(10(11)14-3)5-9(6-8)13-2/h4-6H,1-3H3
InChI key
YXUIOVUOFQKWDM-UHFFFAOYSA-N
Related Categories
General description
Bromination of methyl 3,5-dimethoxybenzoate has been investigated.
Application
Methyl 3,5-dimethoxybenzoate was used as starting reagent in the synthesis of 5,7-dimethoxy-4-methylphthalide, a key intermediate in the synthesis of mycophenolic acid and its analogues.
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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An Improved Synthesis of 5, 7-Dimethoxy-4-methylphthalide, A Key Intermediate in the Synthesis of Mycophenolic Acid.
Makara GM, et al.
Synthetic Communications, 26(10), 1935-1942 (1996)
The bromination of some derivatives of resorcinol.
Cannon JR, et al.
J. Chem. Soc. Sect. C, 3495-3504 (1971)
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