4-Methoxycinnamic acid (Q63391599)

inferred from isomeric SMILES

chemical formula

C₁₀H₁₀O₃

0 references

canonical SMILES

O=C(O)C=CC1=CC=C(OC)C=C1

0 references

isomeric SMILES

COC1=CC=C(C=C1)/C=C/C(=O)O

0 references

melting point

173.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Coffea arabica

1 reference

Development of an HPLC/Diode-Array Detector Method for Simultaneous Determination of Seven Hydroxy-Cinnamic Acids in Green Coffee

Coffea canephora

2 references

ANALYSIS OF HYDROXYCINNAMIC ACIDS OF COFFEE: A COMPARISON OF HIGH PERFORMANCE LIQUID CHROMATOGRAPHY AND CAPILLARY ZONE ELECTROPHORESIS

Development of an HPLC/Diode-Array Detector Method for Simultaneous Determination of Seven Hydroxy-Cinnamic Acids in Green Coffee

Hypenia salzmannii

1 reference

(−)-Salzol, an isopimarane diterpene, and a chalcone from Hyptis salzmanii

Kaempferia galanga

4 references

Studies on crude drugs effective on visceral larva migrans. II. Larvicidal principles in kaempferiae rhizoma

Insecticidal constituents from four species of the zingiberaceae

3-caren-5-one from Kaempferia galanga

Monoamine oxidase inhibitor from the rhizomes of Kaempferia galanga L

Scrophularia spicata

1 reference

Iridoid glycosides from Scrophularia ningpoensis

Ailanthus integrifolia

1 reference

Studies on the constituents of Ailanthus integrifolia

Astianthus viminalis

1 reference

Chemical and Biological Study of Astianthus viminalis

Duranta erecta

1 reference

Chemical Components of the Leaves of Duranta repens LINN.

Eremanthus mollis

1 reference

Three germacranolides and other constituents from Eremanthus species

Illicium verum

1 reference

Effects of p-Methoxycinnamaldehyde from Star Anise and Related Cinnamic Acid Derivatives on Velvetleaf Germination

Murraya euchrestifolia

2 references

Murrayamine-C from murraya euchrestifolia

Murrayamine-C from murraya euchrestifolia

Phlomis floccosa

1 reference

Iridoid glucosides from Phlomis rotata

Scrophularia ningpoensis

2 references

Suppression of SOS-Inducing Activity of Chemical Mutagens by Cinnamic Acid Derivatives fromScrophulia ningpoensisin theSalmonellatyphimuriumTA1535/pSK1002umuTest

Simultaneous determination of four active constituents in the roots of Scrophularia buergeriana by HPLC-DAD and LC-ESI-MS

Spiraea salicifolia

1 reference

Phenolic Compounds from Leaves of Nitraria sibirica

Baccharis subdentata

1 reference

Diterpenes from Baccharis species

Balanophora tobiracola

1 reference

Dihydrochalcones from Balanophora tobiracola

Buddleja asiatica

1 reference

Phenylpropanoid Esters of Rhamnose fromBuddleja asiatica

Campanula glomerata

1 reference

Benzoic and cinnamic acids from Campanula cephalotes

Piper kwashoense

1 reference

Lignans, an amide and anti-platelet activities from Piper philippinum

Piper philippinum

1 reference

Lignans, an amide and anti-platelet activities from Piper philippinum

Rugelia nudicaulis

1 reference

Four oplopanone and bisabolone derivatives from Rugelia nudicaulis

Scrophularia buergeriana

1 reference

Neuroprotective phenylpropanoid esters of rhamnose isolated from roots of Scrophularia buergeriana

Xanthorrhoea preissii

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Xanthorrhoea australis

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Xanthorrhoea resinosa

1 reference

Some Constituents of the Resins of Xanthorrhoea preissii, australis and hastile

Identifiers

InChI

InChI=1S/C10H10O3/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-4+

0 references

1 reference

ChEBI release 2020-09-01

CAS Registry Number

943-89-5

1 reference

https://commonchemistry.cas.org/detail?cas_rn=943-89-5

8 April 2021

PubChem CID

699414

1 reference

ChEBI ID

143736

mapping relation type

exact match

2 references

ChEBI release 2019-10-02

International Chemical Identifier

InChI

InChI=1S/C10H10O3/c1-13-9-5-2-8(3-6-9)4-7-10(11)12/h2-7H,1H3,(H,11,12)/b7-4+

SureChEMBL ID

SCHEMBL58699

2 references

inferred from InChIKey

SCHEMBL58700

2 references

inferred from InChIKey

MSBNK-Fac_Eng_Univ_Tokyo-JP000536

1 reference

MassBank accession ID

SM821404

0 references

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP010387

0 references

0 references

0 references

0 references

0 references

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP005725

0 references

NMRShiftDB structure ID

20073795

1 reference

DSSTox substance ID

DTXSID1046059

2 references

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

DSSTOX compound identifier

DTXCID9026059

0 references

EC number

213-405-4

0 references

ECHA Substance Infocard ID

100.012.187

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.012.187

retrieved

29 December 2019

title

(E)-p-methoxycinnamic acid (English)

quotation

CAS no.: 943-89-5 (English)

1 reference

28 December 2019

METHOXYCINNAMIC ACID (English)

quotation

CAS no.: 943-89-5 (English)

AICS Chemical ID (BEING DELETED)

5929

0 references

Human Metabolome Database ID

HMDB0002040

2 references

inferred from InChIKey

UNII

6G4ML8401A

1 reference