73329-06-3

Basic information

• Product Name: (S)-4-[(1-methylheptyl)oxy]phenol
• Synonyms: (S)-4-[(1-methylheptyl)oxy]phenol
• CAS NO: 73329-06-3
• Molecular Weight: 222.327
• Mol File: 73329-06-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (S)-4-[(1-methylheptyl)oxy]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-[(1-methylheptyl)oxy]phenol(73329-06-3)
• EPA Substance Registry System: (S)-4-[(1-methylheptyl)oxy]phenol(73329-06-3)

Safety Data

• Hazardous Substances Data: 73329-06-3(Hazardous Substances Data)

Upstream product

• 16844-08-9 (S)-(+)-2-chlorooctane 
• 27770-99-6 R(-)-octyl tosylate 
• 5978-70-1 (R)-Octan-2-ol 
• 103-16-2 4-Benzyloxyphenol 
• 6169-06-8 (S)-2-Octanol 
• 108497-36-5 (s)-1-benzyloxy-4-[(1-methylheptyl)oxy]benzene 

Downstream Products

• 129820-05-9 7-Decyloxy-9H-fluorene-2-carboxylic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 
• 129820-08-2 7-Decyloxy-9-oxo-9H-fluorene-2-carboxylic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 
• 129820-06-0 S 2-dodecyloxyfluorene-7-carboxylic acid 4-(2-octyloxy)-phenol ester 
• 129820-09-3 S 2-dodecyloxyfluorenone-7-carboxylic acid 4-(2-octyloxy)-phenyl ester 
• 129820-07-1 7-Tetradecyloxy-9H-fluorene-2-carboxylic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 
• 130005-78-6 9-Oxo-7-tetradecyloxy-9H-fluorene-2-carboxylic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 
• 1351387-34-2 (S)-4-[(1-methylheptyl)oxy]phenol 4'-(6-acryloxyhexyloxy)-[1,1'-biphenyl]-4-carboxylate 
• 137605-15-3 C₃₈H₄₈O₅S 
• 110482-78-5 4-Hydroxy-benzoic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 
• 110482-77-4 4-Benzyloxy-benzoic acid 4-((S)-1-methyl-heptyloxy)-phenyl ester 

Relevant articles and documents

PHOTO-CROSSLINKABLE LIQUID CRYSTAL MONOMERS WITH OPTICAL ACTIVITY

The present invention relates to photo-crosslinkable liquid crystal monomers with optical activity. The liquid crystal monomers contains one chiral center with an acrylate group or terminal diacrylate groups, and terminal dibenzene rings are introduced in order to extend its hard segment for the purpose of getting a wider liquid crystalline phase. By introducing the liquid crystal monomers, the room temperature nematic liquid crystal or the cholesteric liquid crystal may have a better mutual solubility and a wider, steadier structure of liquid crystal. The liquid crystal monomers have the following formula structure:

Long-range chiral induction in chemical systems with helical organization. Promesogenic monomers in the formation of poly(isocyanide)s and in the organization of liquid crystals

The preparation of optically active poly(isocyanide)s derived from chiral promesogenic monomers is reported. Remarkably, the stereogenic carbon atom in the monomer is able to pass its chiral 'information' to the growing polymer backbone which is at least

Ferroelectric and antiferroelectric liquid crystalline phases in some pyridine carboxylic acid derivatives

The synthesis and mesomorphic properties of two series of compounds viz. (S)-(+)-4-(1-methylheptyloxy)phenyl 4′-(6″-alkoxypyridine-3-carbonyloxy)benzoatesand(S)-(+)-1- methylheptyl4-[4′-(6″-alkoxypyridine-3-carbonyloxy)benzoyIoxy]- benzoates are reported; the homologues of the former series exhibit smectic A and smectic C* phases while the derivatives of the latter series show rich polymesomorphism including the antiferroelectric phase. The mesophases have been characterised by using optical polarising microscopy and differential scanning calorimetric methods. Some physical properties such as the spontaneous polarisation, helical pitch, tilt angle and relative permittivity of two derivatives have also been investigated.