95778-33-9

Basic information

• Product Name: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl) -, (E,E)-
• CAS NO: 95778-33-9
• Molecular Formula: C26H40O4
• Molecular Weight: 416.601
• Mol File: 95778-33-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl) -, (E,E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl) -, (E,E)-(95778-33-9)
• EPA Substance Registry System: Benzene, 1,2,3,4-tetramethoxy-5-methyl-6-(3,7,11-trimethyl-2,6,10-dodecatrienyl) -, (E,E)-(95778-33-9)

Safety Data

• Hazardous Substances Data: 95778-33-9(Hazardous Substances Data)

Upstream product

• 24163-93-7 farnesyl bromide 
• 35896-58-3 2,3,4,5-tetramethoxytoluene 
• 87-66-1 2-hydroxyresorcinol 
• 4602-84-0 farnesol 
• 106-44-5 p-cresol 
• 224633-63-0 2,3-dibenzyloxy-1,4-benzoquinone 
• 87997-28-2 2,3,4-tribenzyloxyphenol 
• 7303-36-8 4-amino-pyrogallol; hydrochloride 
• 642-96-6 1,2,3,4-tetrahydroxybenzene 
• 27916-67-2 2,3,4-tris(benzyloxy)benzaldehyde 
• 76088-63-6 4-nitro-1,2,3-trimethoxybenzene 
• 488-64-2 myo-2-inosose 
• 55020-64-9 1,2,3-tris-benzyloxybenzene 
• 21450-56-6 1,2,3,4-tetramethoxybenzene 

Downstream Products

• 1173-76-8 ubiquinone Q₃ 
• 69422-80-6 ubiquinol-3 

Relevant articles and documents

Synthesis of natural product-like polyprenylated phenols and quinones: Evaluation of their neuroprotective activities

Twenty-seven natural product-like polyprenylated phenols and quinones were synthesized and their neuroprotective activity was tested using human monoamine oxidase B (MAO-B) and SH-SY5Y cells. Eight compounds inhibited MAO-B (IC50 values 25 μM

A convergent approach to coenzyme Q

Syntheses of coenzyme Q3-8 are described, as well as related systems such as plastoquinone-5. Preparation of the higher homologues of the ubiquinones relies on two new conjunctive reagents, or "linchpins", each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p-quinone.

Convenient syntheses of vitamin K and coenzyme Q by the coupling of Grignard reagents with allylic phosphate

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