301530-15-4

Basic information

• Product Name: Benzaldehyde, 3-methoxy-4-methyl-5-(phenylmethoxy)-
• CAS NO: 301530-15-4
• Molecular Formula: C16H16O3
• Molecular Weight: 256.301
• Mol File: 301530-15-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 3-methoxy-4-methyl-5-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3-methoxy-4-methyl-5-(phenylmethoxy)-(301530-15-4)
• EPA Substance Registry System: Benzaldehyde, 3-methoxy-4-methyl-5-(phenylmethoxy)-(301530-15-4)

Safety Data

• Hazardous Substances Data: 301530-15-4(Hazardous Substances Data)

Upstream product

• 1011-27-4 3,5-dimethoxy-4-methylbenzaldehyde 
• 34696-31-6 methyl 3,5-bis(benzyloxy)-4-methylbenzoate 
• 75238-29-8 3,5-dihydroxy-4-methylbenzoic acid methyl ester 
• 72922-69-1 methyl 3-(benzyloxy)-5-methoxy-4-methylbenzoate 
• 69660-38-4 5-Hydroxy-3-methoxy-4-methylbenzoesaeure-methylester 
• 28026-96-2 3,5-dihydroxy-4-methylbenzoic acid 

Downstream Products

• 685869-30-1 [(R)-2-Hydroxy-1-(3-{3-methoxy-5-[(S)-2-(2-methoxy-ethoxymethoxy)-1-(2,2,2-trifluoro-acetylamino)-ethyl]-2-methyl-phenoxy}-4-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 685869-32-3 [(R)-2-Hydroxy-1-(4-hydroxy-3-{3-methoxy-5-[(S)-2-(2-methoxy-ethoxymethoxy)-1-(2,2,2-trifluoro-acetylamino)-ethyl]-2-methyl-phenoxy}-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 685869-31-2 [(R)-1-(4-Amino-3-{3-methoxy-5-[(S)-2-(2-methoxy-ethoxymethoxy)-1-(2,2,2-trifluoro-acetylamino)-ethyl]-2-methyl-phenoxy}-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester 
• 685869-29-8 (1S)-N-trifluoroacetyl-1-(3-hydroxy-5-methoxy-4-methylphenyl)-2-((2-methoxyethoxy)methoxy)ethylamine 
• 301530-16-5 3-benzyloxy-5-methoxy-4-methylstyrene 

Relevant articles and documents

Preparation of tricyclic analog as CDE ring model of renieramycin marine natural product by novel photo-induced transformation of 6-methoxy-1,2,3,4-tetrahydroisoquinoline-5,8-dione

2-Acetyl-6-[(benzyloxy)methyl]-9-methoxy-8-methyl-11,11adihydro-2H-pyrazino[1,2-b]isoquinoline-1,4,7,10(3H,6H)-tetraone (11a) was prepared as the CDE ring model of renieramycins, and its novel photo-induced transformation was demonstrated to construct a 1,3-dioxol ring.

Approaches to the fully functionalized DEF ring system of ristocetin A via highly selective ruthenium-promoted SNAr reaction

Ruthenium-promoted intramolecular SNAr reaction has allowed the construction of the fully functionalized 16-membered DEF macrocycle 4 of ristocetin A that incorporates the required arylglycine and arylserine residues as the F and E ring, respectively.