896507-37-2

Basic information

• Product Name: 4-[(S)-2-methylbutyl]-1,3-dimethoxybenzene
• Synonyms: 4-[(S)-2-methylbutyl]-1,3-dimethoxybenzene
• CAS NO: 896507-37-2
• Molecular Weight: 208.301
• Mol File: 896507-37-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-[(S)-2-methylbutyl]-1,3-dimethoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(S)-2-methylbutyl]-1,3-dimethoxybenzene(896507-37-2)
• EPA Substance Registry System: 4-[(S)-2-methylbutyl]-1,3-dimethoxybenzene(896507-37-2)

Safety Data

• Hazardous Substances Data: 896507-37-2(Hazardous Substances Data)

Upstream product

• 534-00-9 (S)-2-methylbutyl bromide 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 
• 151-10-0 1,3-Dimethoxybenzene 

Downstream Products

• 896507-40-7 4-bromo-6-[(S)-2-methylbutyl]-1,3-dimethoxybenzene 
• 896507-43-0 5-[(S)-2-methylbutyl]-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolyl)-2,4-dimethoxybenzene 
• 896507-38-3 5-[(S)-2-methylbutyl]-2,4,4',6',4'',6'',2''',4'''-octamethoxy-1,1':3',1'':3'',1'''-quaterphenyl 
• 896507-41-8 5-bromo-5'''-[(S)-2-methylbutyl]-2,4,4',6',4'',6'',2''',4'''-octamethoxy-1,1':3',1'':3'',1'''-quaterphenyl 
• 896507-44-1 5'''-[(S)-2-methylbutyl]-2,4,4',6',4'',6'',2''',4'''-octamethoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolyl)-1,1':3',1'':3'',1'''-quaterphenyl 
• 906646-96-6 5-[(S)-2-methylbutyl]-2,4,4',6',4'',6'',4''',6''',4'''',6'''',4''''',6''''',2'''''',4''''''-tetradecamethoxy-1,1':3',1'':3'',1''':3''',1'''':3'''',1''''':3''''',1''''''-septiphenyl 
• 896507-45-2 5-iodo-5''''''-[(S)-2-methylbutyl]-2,4,4',6',4'',6'',4''',6''',4'''',6'''',4''''',6''''',2'''''',4''''''-tetradecamethoxy-1,1':3',1'':3'',1''':3''',1'''':3'''',1''''':3''''',1''''''-septiphenyl 

Relevant articles and documents

Oligoresorcinols fold into double helices in water

We report the first double helices with a controlled helicity in water based on oligoresorcinols as a new, simplest water-soluble structural motif. The molecular strands of the oligoresorcinols self-assemble into double helices with the aid of aromatic interactions in water as characterized by 1H NMR and absorption spectroscopies together with the X-ray crystallographic study of the pentamer. The double helix formation is sensitive to the chain length, solvent composition, and temperature. Moreover, a bias in the screw sense of the double helices was achieved by covalently attaching chiral substituents to both ends of the molecular strands. Copyright