P-ANISALDEHYDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C8H8O2
Molecular Weight	136.1479
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

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

InChI

InChIKey=ZRSNZINYAWTAHE-UHFFFAOYSA-N

InChI=1S/C8H8O2/c1-10-8-4-2-7(6-9)3-5-8/h2-6H,1H3

HIDE SMILES / InChI

Approval Year

PubMed

Show entries

Title	Date	PubMed
Novel hypotensive agents from Verbesina caracasana. 8. Synthesis and pharmacology of (3,4-dimethoxycinnamoyl)-N(1)-agmatine and synthetic analogues.	2001 Aug 30	11520203
New 4-methoxybenzoyl derivatives from the ascidian Polycarpa aurata.	2001 Dec	11754611
Helicobacter pylori-binding gangliosides of human gastric adenocarcinoma.	2001 Nov	11744628
Biosynthesis of p-anisaldehyde by the white-rot basidiomycete Pleurotus ostreatus.	2002	16233188
Characterization of the Saccharomyces cerevisiae YMR318C (ADH6) gene product as a broad specificity NADPH-dependent alcohol dehydrogenase: relevance in aldehyde reduction.	2002 Jan 1	11742541

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Name

Type

Language

ANISALDEHYDE

Preferred Name

English

P-ANISALDEHYDE

Common Name

English

P-ANISALDEHYDE [MI]

Common Name

English

P-FORMYLANISOLE

Common Name

English

CRATEGINE

Common Name

English

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Classification Tree

Code System

Code

FUNCTIONAL CLASSIFICATION

JECFA EVALUATION

P-METHOXYBENZALDEHYDE

Subpart F--Flavoring Agents and Related Substances

CFR

21 CFR 172.515

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Code System

Code

Type

Description

FDA UNII

9PA5V6656V

PRIMARY

PUBCHEM

31244

PRIMARY

EPA CompTox

DTXSID2026997

PRIMARY

DAILYMED

9PA5V6656V

PRIMARY

EVMPD

SUB37593

PRIMARY

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SUBSTANCE RECORD


					9PA5V6656V

P-ANISALDEHYDE

SMILES

InChI

Approval Year

PubMed

Patents