42933-32-4

Basic information

• Product Name: 3,6,7-trimethyl-2,6-octadien-1-ol
• Synonyms: 3,6,7-trimethyl-2,6-octadien-1-ol
• CAS NO: 42933-32-4
• Molecular Formula: C11H20O
• Molecular Weight: 168.2759
• EINECS: 256-009-7
• Mol File: 42933-32-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 246.9°C at 760 mmHg
• Flash Point: 92.6°C
• Appearance: /
• Density: 0.866g/cm³
• Vapor Pressure: 0.00433mmHg at 25°C
• Refractive Index: 1.469
• CAS DataBase Reference: 3,6,7-trimethyl-2,6-octadien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6,7-trimethyl-2,6-octadien-1-ol(42933-32-4)
• EPA Substance Registry System: 3,6,7-trimethyl-2,6-octadien-1-ol(42933-32-4)

Safety Data

• Hazardous Substances Data: 42933-32-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H20O/c1-9(2)11(4)6-5-10(3)7-8-12/h7,12H,5-6,8H2,1-4H3/b10-7+

Upstream product

• 58307-67-8 3,6,7-trimethyl-6-octen-1-en-3-ol 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 127-09-3 sodium acetate 
• 408328-44-9 3,6,7-trimethyl-6-octen-1-en-3-yl acetate 
• 1891-67-4 3,6,7-trimethylocta-2,6-dienal 
• 131534-46-8 2-acetyl-4,5-dimethyl-hex-4-enoic acid ethyl ester 
• 5072-70-8 1-bromo-2,3-dimethyl-2-butene 
• 19310-95-3 2,3-dimethylbut-2-en-1-ol 
• 13979-28-7 ethyl 2,3-dimethylbut-2-enoate 
• 408319-02-8 3-acetoxy-3,6,7-trimethyl-oct-6-enoic acid ethyl ester 
• 408318-64-9 3-hydroxy-3,6,7-trimethyl-oct-6-enoic acid ethyl ester 
• 52567-96-1 3,6,7-trimethyl-oct-6-en-1-yn-3-ol 
• 130627-71-3 6-benzoylsulfonyl-3,7-dimethylocta-2E,7-dien-1-yl acetate 

Downstream Products

• 72074-85-2 (+-)-4t-(2,5c,6,6-tetramethyl-cyclohex-2-en-r-yl)-but-3-en-2-one 
• 18445-02-8 (E)-6,9,10-trimethylundeca-5,9-dien-2-one 

Relevant articles and documents

Rerouting and Improving Dauc-8-en-11-ol Synthase from Streptomyces venezuelae to a High Yielding Biocatalyst

The dauc-8-en-11-ol synthase from Streptomyces venezuelae was investigated for its catalytic activity towards alternative terpene precursors, specifically designed to enable new cyclisation pathways. Exchange of aromatic amino acid residues at the enzyme surface by site-directed mutagenesis led to a 4-fold increase of the yield in preparative scale incubations, which likely results from an increased enzyme stability instead of improved enzyme kinetics.

Synthesis of teleocidins A, B and their congeners. Part 3. Synthesis of dihydroteleocidin B-4 (dihydroteleocidin B), teleocidin B-3 and teleocidin B-4

Details of the synthesis method of the tumor promoters teleocidin B-3 (3), teleocidin B-4 (4) and dihydroteleocidin B-4 (9) (=dihydroteleocidin B) from (S)- and (R)-methyl N-methyl-N-[7-(3,6,7-trimethyl-1,6-octadien-3-yl)-4-indolyl]-L-valinates (20b and 20a) are presented.

A new synthesis of irones IV (1) 6-substituted geraniols, 6-substituted ionones and tetrahydrofuran analogs

-