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Merck
CN

426091

2,5-二羟基苯甲酸甲酯

99%

别名:

龙胆酸甲酯

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关于此项目

线性分子式:
(HO)2C6H3CO2CH3
化学文摘社编号:
分子量:
168.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-427-8
MDL number:
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产品名称

2,5-二羟基苯甲酸甲酯, 99%

InChI key

XGDPKUKRQHHZTH-UHFFFAOYSA-N

InChI

1S/C8H8O4/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4,9-10H,1H3

SMILES string

COC(=O)c1cc(O)ccc1O

assay

99%

mp

86-88 °C (lit.)

functional group

ester

Quality Level

Application

Methyl 2,5-dihydroxybenzoate (methyl gentisate) may be used as a starting material in the synthesis of euonyminol.

General description

Methyl 2,5-dihydroxybenzoate (methyl gentisate) is an alkyl ester of gentisic acid. It is reported to show less cytotoxic and mutagenic activity than hydroquinone with a potential to inhibit melanogenesis. It has been synthesized from 2,5-dihydroxybenzoic acid. The crystal structure of the molecule was found to be planar.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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E V Curto et al.
Biochemical pharmacology, 57(6), 663-672 (1999-02-26)
To discover safe and effective topical skin-lightening agents, we have evaluated alkyl esters of the natural product gentisic acid (GA), which is related to our lead compound methyl gentisate (MG), and four putative tyrosinase inhibitors, utilizing mammalian melanocyte cell cultures
Methyl 2, 5-dihydroxybenzoate.
Brown CL, et al.
Acta Crystallographica Section E, Structure Reports Online, 59(5), 630-631 (2003)
Total Synthesis of (.+-.)-Euonyminol, the Sesquiterpenoid Nucleus of Cathedulin K-19, via an Epoxide Cascade Cyclization.
White JD, et al.
Journal of the American Chemical Society, 117(38), 9780-9781 (1995)

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