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168793

Sigma-Aldrich

Methyl 3,5-dimethoxybenzoate

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25 G
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25 G
$93.50

About This Item

Linear Formula:
(CH3O)2C6H3CO2CH3
CAS Number:
2150-37-0
Molecular Weight:
196.20
EC Number:
218-423-6
MDL number:
MFCD00008432
UNSPSC Code:
12352100
PubChem Substance ID:
24850255
NACRES:
NA.22

$93.50

List Price$187.00Save 50%
Web-Only Promotion

Available to ship onMay 01, 2025Details

Request a Bulk Order

Quality Level

100

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[1].

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[2].

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
STBL1306
STBK7858
STBC8660V
09111TB
03527JE

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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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