34883-08-4

Basic information

• Product Name: 4-Methoxy-6-methylsalicylaldehyde
• Synonyms: 2-Hydroxy-4-methoxy-6-methylbenzaldehyde;4-Methoxy-6-methylsalicylaldehyde;Everninaldehyde
• CAS NO: 34883-08-4
• Molecular Formula: C₉H₁₀O₃
• Molecular Weight: 166.17
• Mol File: 34883-08-4.mol
• Article Data: 5

Chemical Properties

• Melting Point: 65 °C
• Boiling Point: 294.9±35.0 °C(Predicted)
• Appearance: /
• Density: 1.188±0.06 g/cm3(Predicted)
• PKA: 7.91±0.15(Predicted)
• CAS DataBase Reference: 4-Methoxy-6-methylsalicylaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methoxy-6-methylsalicylaldehyde(34883-08-4)
• EPA Substance Registry System: 4-Methoxy-6-methylsalicylaldehyde(34883-08-4)

Safety Data

• Hazardous Substances Data: 34883-08-4(Hazardous Substances Data)

Upstream product

• 487-69-4 2,4-dihydroxy-6-methylbenzaldehyde 
• 74-88-4 methyl iodide 
• 7149-90-8 2,4-dimethoxy-6-methyl-benzaldehyde 
• 77-78-1 dimethyl sulfate 
• 3209-13-0 O-methylorcinol 
• 4179-19-5 1,3-dimethoxy-5-methylbenzene 
• 50-00-0 formaldehyd 

Downstream Products

• 872304-60-4 3,6-dihydroxy-4-methoxy-2-methyl-benzaldehyde 
• 59263-71-7 2-acetoxy-4-methoxy-6-methyl-benzaldehyde 
• 110451-94-0 2-(2,2-diethoxyethoxy)-4-methoxy-6-methylbenzaldehyde 
• 59342-30-2 2-Benzyloxy-4-methoxy-6-methyl-benzaldehyde 
• 27161-92-8 schizopeltic acid 
• 84161-45-5 benzyl schizopeltate 
• 84161-42-2 benzyl 1,7-dimethoxy-3,9-dimethyldibenzofuran-4-carboxylate 
• 84161-43-3 benzyl 8-formyl-1,7-dimethoxy-3,9-dimethyldibenzofuran-4-carboxylate 
• 60059-02-1 2-methyl-3,4,6-trimethoxybenzaldehyde 
• 855751-99-4 2-ethoxycarbonyloxy-4-methoxy-6-methyl-benzoic acid 
• 3542-22-1 Evernsaeuremethylester 
• 61035-71-0 2-acetoxy-4-methoxy-6-methyl-benzoic acid 
• 858842-86-1 2-ethoxy-4-methoxy-6-methyl-benzoic acid 
• 59311-42-1 4-Hydroxy-2-(2-hydroxy-4-methoxy-6-methyl-phenoxy)-6-methyl-benzoic acid 

Relevant articles and documents

1,4,2-Dioxazines or N-Acyl Isoxazolidines from Organoselenium-induced Cyclisation of O-Allyl Hydroxamic Acids

O-Allyl hydroxamic acids easily give rise to organoselenium-induced cyclisation reactions to afford phenylseleno-substituted 1,4,2-dioxazines or N-acyl isoxazolidines as the kinetically or thermodynamically controlled products, respectively.

PYRIMIDINE DERIVATIVES AS PGE2 RECEPTOR MODULATORS

The present invention relates to pyrimidine derivatives of formula (I) wherein (R1)n, R3, R4a, R4b, R5a, R5b and Ar1 are as described in the description and their use in the treatment of cancer by modulating an immune response comprising a reactivation of the immune system in the tumor. The invention further relates to novel benzofurane and benzothiophene derivatives of formula (II) and their use as pharmaceuticals, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as modulators of the prostaglandin 2 receptors EP2 and/or EP4.

Naturally Occuring Dibenzofurans. Part 2. The Synthesis of Schizopeltic Acid

The structure of schizopeltic acid as 1,7-dimethoxy-8-methoxycarbonyl 3,9-dimethyldibenzofuran-4-carboxylic acid (1) has been confirmed by rational synthesis. 6-Methoxy-4-methylbenzofuran-2-carbaldehyde (10), available from 3,5-dimethoxytoluene (4) in six