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o-Anisaldehyde, 98%|279079|135-02-4

o-Anisaldehyde, 98%

Cat. No JK279079_5_G
J&K Chemical

Product Information

Product Name
o-Anisaldehyde, 98%
Brand Name
J&K
Product Number
279079
CAS
135-02-4
Molecular Formula
C8H8O2
Molecular Weight
136.15
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
2-Methoxybenzaldehyde
PubChem CID
8658
IUPAC Name
2-methoxybenzaldehyde
InChI Key
PKZJLOCLABXVMC-UHFFFAOYSA-N
SMILES
COC1=CC=CC=C1C=O

Properties

Density
1.127
Melting Point
34-40
Boiling Point
238
Flash Point
118

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

A Herbivory-Induced Volatile Disrupts Host Selection by Chilli Thrips, Scirtothrips dorsalis, on Strawberry
Publication Name: Journal of Chemical Ecology
Publication Date: 2026-02-19
DOI: 10.1007/s10886-026-01698-3

Exploring MAO inhibitory activity of 5-hydroxy regioisomers of hispidol’s analogs leads to identification of novel highly selective MAO-B open-conformation inhibitors
Publication Name: Molecular Diversity
Publication Date: 2026-02-01
DOI: 10.1007/s11030-025-11464-4

Synthesis and integrative multimodal evaluation of cholic acid-based hydrazone conjugates: in vitro, in silico, and in vivo studies
Publication Name: Naunyn-Schmiedeberg's Archives of Pharmacology
Publication Date: 2026-01-30
DOI: 10.1007/s00210-026-04991-w

The Cell-Specific Effects of the Human Remyelination-Promoting rHIgM22 on Sphingolipid Metabolism in Cultured Glial Cells
Publication Name: Neurochemical Research
Publication Date: 2026-01-24
DOI: 10.1007/s11064-025-04657-8

Development of novel catalytic synthetic strategies for Henry reaction: a review
Publication Name: Journal of the Iranian Chemical Society
Publication Date: 2026-01-24
DOI: 10.1007/s13738-025-03314-9

o-Anisaldehyde, 98%

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