90432-92-1

Basic information

• Product Name: 1,3-Dioxolane, 2-methyl-2-[4-methyl-5-(phenylmethoxy)pentyl]-
• CAS NO: 90432-92-1
• Molecular Formula: C17H26O3
• Molecular Weight: 278.392
• Mol File: 90432-92-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-Dioxolane, 2-methyl-2-[4-methyl-5-(phenylmethoxy)pentyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxolane, 2-methyl-2-[4-methyl-5-(phenylmethoxy)pentyl]-(90432-92-1)
• EPA Substance Registry System: 1,3-Dioxolane, 2-methyl-2-[4-methyl-5-(phenylmethoxy)pentyl]-(90432-92-1)

Safety Data

• Hazardous Substances Data: 90432-92-1(Hazardous Substances Data)

Upstream product

• 38237-34-2 2-Methyl-2-(4-methyl-4-pentenyl)-1,3-dioxolane 
• 15580-05-9 5-(2-methyl-1,3-dioxolan-2-yl)-2-pentanone 

Downstream Products

• 77878-59-2 ethyl 8-(benzyloxy)-3,7-dimethyl-2-octenoate 
• 77878-33-2 1-(benzyloxy)-2,6-dimethyl-10-oxoundec-6-ene 
• 77878-12-7 8-(benzyloxy)-3,7-dimethyl-2-octenol 
• 77878-55-8 (E)-2-Acetyl-10-benzyloxy-5,9-dimethyl-dec-4-enoic acid ethyl ester 
• 67441-54-7 (1RS,4SR,5RS)-4-(5-hydroxy-4,8-dimethyl-7-nonen-1-yl)-4-methyl-3,8-dioxabicyclo<3.2.1>octane-1-acetic acid 
• 77878-09-2 11-(benzyloxy)-1-bromo-6,10-dimethyl-2-oxoundec-5-ene 
• 77878-32-1 11-benzyloxy-6,10-dimethyl-2-trimethylsiloxy-undec-1,5-diene 
• 77878-43-4 7-benzyloxy-2-[2-bromomethyl-2-methoxy-tetrahydrofuran-5-yl]-6-methyl-heptan-2-ol 
• 77878-39-8 11-benzyloxy-1-bromo-6,10-dimethyl-5,6-epoxy-undecan-2-one 
• 77878-41-2 7-Benzyloxy-2-(2-bromomethyl-2-hydroxy-tetrahydrofuran-5-yl)6-methyl-heptan-2-ol 
• 77878-62-7 (1RS,4RS,5SR)-4-<5-(Benzyloxy)-4-methylpentyl>-1-methoxy-4-methyl-3,8-dioxabicyclo<3.2.1>octane 
• 77878-07-0 ((E)-8-Chloro-2,6-dimethyl-oct-6-enyloxymethyl)-benzene 
• 77878-52-5 1(Benzyloxy)-2-methyl-6-oxoheptane 

Relevant articles and documents

(1RS,4SR,5RS)-4-(5-Hydroxy-4,8-dimethyl-7-nonen-1-yl)-4-methyl-3,8-dioxabicyclooctane-1-acetic Acid from Geraniol

(E)-Geraniol (4) has been converted via 13 steps involving epoxidations, hydrolytic epoxide ring opening, and two ring closures to the key intermediate 3,8-dioxabicyclooctane alcohol 10 having stereochemical integrity at all three centers of asymmetry.Extension of the three-carbon side chain of 10 and attachment of the acetic acid side chain at C-1 in nine steps completed the geraniol-based total synthesis of the zoapatanol related bicyclic acid 3.The total synthesis of 3 from the ketal-ketone 5 has also been described.