1805-67-0

Basic information

• Product Name: 5-METHYLISOPHTHALALDEHYDE
• Synonyms: 5-METHYLISOPHTHALALDEHYDE;5-methyl-1,3-Benzenedicarboxaldehyde
• CAS NO: 1805-67-0
• Molecular Formula: C₉H₈O₂
• Molecular Weight: 148.15862
• Mol File: 1805-67-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-METHYLISOPHTHALALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHYLISOPHTHALALDEHYDE(1805-67-0)
• EPA Substance Registry System: 5-METHYLISOPHTHALALDEHYDE(1805-67-0)

Safety Data

• Hazardous Substances Data: 1805-67-0(Hazardous Substances Data)

Usage

Description

5-METHYLISOPHTHALALDEHYDE is a chemical compound with the molecular formula C9H8O2, characterized by its yellow-brown liquid appearance and a strong, unpleasant odor.
Used in Fragrance Industry:
5-METHYLISOPHTHALALDEHYDE is used as a fragrance ingredient for its distinctive scent, contributing to the formulation of perfumes, soaps, and detergents.
Used in Chemical Production:
5-METHYLISOPHTHALALDEHYDE is used as a raw material in the production of polymers, resins, and dyes, playing a crucial role in the synthesis of various industrial products.

Upstream product

• 2747-53-7 3-methyl-3-penten-2-ol 
• 68-12-2 N,N-dimethyl-formamide 
• 4798-58-7 (E)-hex-4-en-3-ol 
• 688-99-3 5-hexen-3-ol 
• 29478-26-0 (S,R)-trans-3-hexen-2-ol 
• 4798-44-1 1-hexene-3-ol 
• 31673-44-6 3-methylcyclohexa-2,5-dienecarboxylic acid 
• 27711-63-3 1,3-bis-(hydroxymethyl)-5-methylbenzene 
• 17649-58-0 5-Methylisophthalsaeure-dimethylester 

Downstream Products

• 1805-68-1 opt.-inakt. 5-Methyl-1,3-bis-(1-hydroxy-isopentyl)-benzol 
• 74126-23-1 5-methylbenzene-1,3-dicarbaldehyde bis-(p-tolylsulphonylhydrazone) 
• 255375-93-0 5-methylisophthalaldehyde bis(propane-1,3-diyl dithioacetal) 
• 258834-70-7 1,3-bis(2,2':6',2''-terpyridin-4'-yl)-5-methylbenzene 
• 74126-24-2 5-methylbenzene-1,3-dicarbaldehyde bis-(p-tolylsulphonylhydrazone) - benzene 1:2 complex 
• 1805-69-2 5-Methyl-1,3-diisopentyl-benzol 
• 1850-40-4 4-Nitro-5-methyl-1,3-diisopentyl-benzol 
• 1850-41-5 6-Methyl-2,4-diisopentyl-anilin 
• 1805-71-6 N-<2,2-Dimethyl-butyryl>-6-methyl-2,4-diisopentyl-anilid 
• 708974-78-1 C₉H₁₀N₂O₂ 
• 1361477-51-1 C₂₅H₂₈O₄ 
• 1335292-96-0 C₂₅H₂₀O₂ 

Relevant articles and documents

DESIGN and SYNTHESIS of 1,3-BIS(3-(TRIFLUOROMETHYL)- DIAZIRIN-3-YL)PHENYLALANINE for EFFICIENT PHOTOCROSS- LINKING

Photoreactive a-amino acids are powerful chemical tools for elucidating interactions in protein networks. Typically, photophores are required for stability and generation of high-reactive species. Additionally, orientation of photophores is one of the significant issues for performing photoaffinity labeling. Therefore, we rationally designed a bis-diazirinyl-phenylalanine for which photocross- linking efficiency could be increased. In this study, we synthesized a new 1,3-bis(3-(trifluoromethyl)diazirin-3-yl)phenylalanine and demonstrated further study in terms of photoactivation.

AMINOGUANIDINE HYDRAZONES AS RETROMER STABILIZERS USEFUL FOR TREATING NEUROLOGICAL DISEASES

The present invention relates to novel aminoguanidine hydrazone-derivatives of Formula (I) which are effective as retromer stabilizers and useful as neuroprotecting drugs. The invention also relates to pharmaceutical compositions comprising the compounds and their use in therapy and diagnostic.

Conversion of 1,4-Dihydrobenzoic Acids to Polyformylbenzenes under Vilsmeier Reaction Conditions

1,4-Dihydrobenzoic acids 1a-e are converted by a one-pot reaction to benzene- mono-, di- and tricarboxaldehydes under Vilsmeier reaction conditions in yields ranging from 6 to 65percent.The same methodology also serves to give naphthalene-1,3-dicarboxaldehyde (2f) from 1,4-dihydro-1-naphthoic acid (1f) in 91percent yield.