Isovanillic acid (Q1674563)

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

chemical formula

C₈H₈O₄

1 reference

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

canonical SMILES

COC1=C(C=C(C=C1)C(=O)O)O

1 reference

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

melting point

253.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Pinus pinaster

1 reference

Carboxylic Acids of Moroccan Pinus Pinaster Bark Extract

Crocus sativus

3 references

Antityrosinase principles and constituents of the petals of Crocus sativus

Antityrosinase principles and constituents of the petals of Crocus sativus

Antityrosinase principles and constituents of the petals of Crocus sativus

Parmentiera cereifera

1 reference

Phenolic acid glycosides from Parmentiera cereifera Seem. (Candle tree)

Annona cherimola

2 references

Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola

Cheritamine, A NewN-Fatty Acyl Tryptamine and Other Constituents from the Stems ofAnnona cherimola

Annona purpurea

2 references

Four alkaloids from Annona cherimola.

New alkaloids from Annona purpurea

Aristolochia gehrtii

1 reference

Alkamides and phenethyl derivatives from Aristolochia gehrtii

Aristolochia heterophylla

1 reference

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Aristolochia kaempferi

1 reference

The constituents of the root and stem of Aristolochia heterophylla Hemsl

Cassia fistula

2 references

The Chemical Constituents from the Aril of Cassia FistulaL.

The Chemical Constituents from the Aril of Cassia FistulaL.

Ginkgo biloba

1 reference

HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY AND THIN-LAYER CHROMATOGRAPHY OF PHENOLIC ACIDS FROM GINKGO BILOBA L. LEAVES COLLECTED WITHIN VEGETATIVE PERIOD

Hypericum erectum

1 reference

Chemical constituents of Hypericum erectum Thunb

avocado

1 reference

Total phenolics and high-performance liquid chromatography of phenolic acids of avocado

Scrophularia frutescens

3 references

Antibacterial activity of the phenolic acids fractions of Scrophularia frutescens and Scrophularia sambucifolia

Anti-inflammatory activity in rats and mice of phenolic acids isolated from Scrophularia frutescens

Cytostatic Activity of Some Phenolic Acids of Scrophularia frutescens L. var. frutescens

Soroseris hookeriana

2 references

New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides

New antimicrobial mono- and sesquiterpenes from Soroseris hookeriana subsp. erysimoides

Zanthoxylum bungeanum

1 reference

Effects of extracts ofZanthoxylum fruit and their constituents on spontaneous beating rate of myocardial cell sheets in culture

Bauhinia glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Streptomyces

1 reference

Streptomyces sp. MUM273b: A mangrove-derived potential source for antioxidant and UVB radiation protectants

Imperata cylindrica

1 reference

Chemical interaction in the invasiveness of cogongrass (Imperata cylindrica (L.) Beauv.).

Perilla frutescens var. crispa

1 reference

Structural characterization of phenolic antioxidants from purple perilla (Perilla frutescens var. acuta) leaves

Acacia confusa

1 reference

Phenolic antioxidants from the heartwood of Acacia confusa.

Cota palaestina

1 reference

Sesquiterpene Lactones fromAnthemis melanolepisand Their Antibacterial and Cytotoxic Activities. Prediction of Their Pharmacokinetic Profile

Cacia confusa

1 reference

Phenolic antioxidants from the heartwood of Acacia confusa.

Calophyllum polyanthum

1 reference

Two new 4-arylcoumarins from the seeds of Calophyllum polyanthum

Centaurea spruneri

1 reference

Antimicrobial activity of secondary metabolites isolated from Centaurea spruneri Boiss.& Heldr

Euphorbia decipiens

1 reference

Structure elucidation of two new unusual monoterpene glycosides from Euphorbia decipiens, by 1D and 2D NMR experiments

Euphorbia polycaulis

1 reference

Structure elucidation of two new unusual monoterpene glycosides from Euphorbia decipiens, by 1D and 2D NMR experiments

Leucaena leucocephala

1 reference

Secondary metabolites from Leucaena leucocephala

Muntingia calabura

1 reference

New dihydrochalcones and anti-platelet aggregation constituents from the leaves of Muntingia calabura

Santalum album

1 reference

Aromatic constituents from the heartwood of Santalum album L

Scrophularia ningpoensis

1 reference

A sugar ester and an iridoid glycoside from Scrophularia ningpoensis

Synsepalum dulcificum

1 reference

Chemical constituents from the roots of Synsepalum dulcificum

Vincetoxicum hemsleyanum

2 references

Chemical Constituents from the Roots of Morinda officinalis

Chemical constituents from the roots of Biondia chinensis

Galinsoga ciliata

1 reference

Polyphenolic compounds of Scabiosa caucasica

Galinsoga quadriradiata

1 reference

Polyphenolic compounds of Scabiosa caucasica

Cheniella glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Identifiers

InChI

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

1 reference

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

2 references

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

ChEBI release 2020-09-01

2 references

3-hydroxy-4-methoxybenzoic acid (English)

7 October 2016

https://commonchemistry.cas.org/detail?cas_rn=645-08-9

9 April 2021

1 reference

3-Hydroxy-4-methoxybenzoic acid (English)

7 October 2016

2 references

3-HYDROXY-4-METHOXYBENZOIC ACID (English)

7 October 2016

Reaxys registry number

2208365

1 reference

3-hydroxy-4-methoxybenzoic acid (English)

7 October 2016

ChEBI ID

63798

mapping relation type

2 references

3-hydroxy-4-methoxybenzoic acid (English)

7 October 2016

International Chemical Identifier

InChI

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

1 reference

ISOVANILLIC ACID (English)

7 October 2016

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP011443

1 reference

MassBank accession ID

0 references

SPLASH

splash10-0gb9-0900000000-660260d6741ecd0596f0

0 references

NMRShiftDB structure ID

20039584

1 reference

DSSTox substance ID

DTXSID40214745

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.010.392

27 December 2018

ECHA Substance Infocard ID

3-hydroxy-p-anisic acid (English)

quotation

CAS no.: 645-08-9 (English)

100.010.392

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.010.392

27 December 2018

Human Metabolome Database ID

3-hydroxy-p-anisic acid (English)

quotation

CAS no.: 645-08-9 (English)

HMDB0060003

2 references

based on heuristic

inferred from InChIKey

KNApSAcK ID

C00029502

2 references

based on heuristic

inferred from InChIKey

UNII

A8D1DUX2PR

1 reference