71135-48-3

Basic information

• Product Name: (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol
• Synonyms: (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol
• CAS NO: 71135-48-3
• Molecular Formula: C₂₂H₃₂O₂
• Molecular Weight: 328.48828
• Mol File: 71135-48-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Amber Vial, -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform, Dichloromethane, Ethyl Acetate
• CAS DataBase Reference: (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol(71135-48-3)
• EPA Substance Registry System: (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol(71135-48-3)

Safety Data

• Hazardous Substances Data: 71135-48-3(Hazardous Substances Data)

Usage

Description

(2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol is a naturally occurring organic compound that belongs to the class of terpenoids. It is characterized by its unique molecular structure, featuring three double bonds and a phenylmethoxy group. (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol is known for its diverse range of applications in various industries, particularly in the pharmaceutical and chemical sectors.

Uses

Used in Pharmaceutical Industry:
(2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol is used as a key intermediate in the synthesis of coenzymes Q, vitamin K, and polyprenylquinones. These compounds play crucial roles in various biological processes, such as cellular respiration, energy production, and blood clotting. (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol's unique structure allows it to be easily modified and incorporated into these complex molecules, making it an essential component in the development of pharmaceutical products.
Used in Chemical Industry:
In the chemical industry, (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol serves as a versatile building block for the synthesis of various specialty chemicals and materials. Its unique structure and functional groups make it suitable for use in the production of fragrances, flavorings, and other fine chemicals. Additionally, its ability to form stable complexes with metal ions makes it a potential candidate for use in catalysis and other chemical processes.

Upstream product

• 71135-45-0 C₂₈H₃₆OS 
• 56506-81-1 (2E,6E)-1-(benzyloxy)-3,7,11-trimethyl-2,6,10-dodecatriene 
• 106-28-5 Farnesol 
• 100-44-7 benzyl chloride 

Downstream Products

• 13190-97-1 solanesol 
• 71135-59-6 C₆₆H₉₂O₅S₂ 
• 71135-58-5 1-((2E,6E,10E,14E,18E,22E)-24-Benzyloxy-1-bromo-2,6,10,14,18,22-hexamethyl-tetracosa-2,6,10,14,18,22-hexaene-12-sulfonyl)-4-methyl-benzene 
• 71135-57-4 (2E,6E,10E,14E,18E,22E)-24-Benzyloxy-2,6,10,14,18,22-hexamethyl-12-(toluene-4-sulfonyl)-tetracosa-2,6,10,14,18,22-hexaen-1-ol 
• 273205-50-8 All-trans-ω-acetoxyfarnesyl benzyl ether 
• 68731-64-6 (2E,6E,10E)-1-Benzyloxy-3,7,11-trimethyl-12-chlorododeca-2,6,10-triene 
• 733010-74-7 (6E,10E)-(S)-12-Benzyloxy-2,6,10-trimethyl-dodeca-1,6,10-trien-3-ol 
• 733010-75-8 (4E,8E)-(S)-10-Benzyloxy-4,8-dimethyl-1-((R)-2-methyl-oxiranyl)-deca-4,8-dien-1-ol 
• 733010-76-9 (R)-2-[(4E,8E)-(S)-10-Benzyloxy-1-(1-ethoxy-ethoxy)-4,8-dimethyl-deca-4,8-dienyl]-2-methyl-oxirane 
• 733010-80-5 [(4R,5S)-5-((3E,7E)-9-Benzyloxy-3,7-dimethyl-nona-3,7-dienyl)-2,2,4-trimethyl-[1,3]dioxolan-4-yl]-acetonitrile 
• 733010-78-1 (7E,11E)-(3R,4S)-13-Benzyloxy-3,4-dihydroxy-3,7,11-trimethyl-trideca-7,11-dienenitrile 
• 733010-81-6 2-[(4R,5S)-5-((3E,7E)-9-Benzyloxy-3,7-dimethyl-nona-3,7-dienyl)-2,2,4-trimethyl-[1,3]dioxolan-4-yl]-ethanol 
• 733010-77-0 (7E,11E)-(3R,4S)-13-Benzyloxy-4-(1-ethoxy-ethoxy)-3-hydroxy-3,7,11-trimethyl-trideca-7,11-dienenitrile 
• 733010-82-7 {2-[(4R,5S)-5-((3E,7E)-9-Benzyloxy-3,7-dimethyl-nona-3,7-dienyl)-2,2,4-trimethyl-[1,3]dioxolan-4-yl]-ethoxy}-tert-butyl-dimethyl-silane 

Relevant articles and documents

Synthesis and NMR characterisation of novel highly cyclised polyprenoid hydrocarbons from sediments

We report here on the identification of two novel hexacyclic alkanes (C33 and C35) occurring in bitumen. The C35 compound 1 was identified by comparison with a standard obtained by synthesis involving a biomimetic proton-induced extensive cyclisation of an acyclic heptaprenoid. This cascade cyclisation allows the formation of eleven asymmetric centres present in the natural compound in only one step. The C33 analogue 2 was identified by NMR studies after isolation from the saturated hydrocarbon fraction of a bituminous rock. Both compounds are "orphan" molecular fossils of biological lipids of unknown origin formed by the extensive cyclisation of higher regular polyprenoids.

Regio- and stereoselective synthesis of coenzymes Q(n) (n=2-10), vitamin K, and related polyprenylquinones

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