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1065-31-2

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  • 2,5-Cyclohexadiene-1,4-dione,2-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaen-1-yl]-5,6-dimethoxy-3-methyl-

    Cas No: 1065-31-2

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  • 2,5-Cyclohexadiene-1,4-dione,2-[(2E,6E,10E,14E,18E)-3,7,11,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaen-1-yl]-5,6-dimethoxy-3-methyl- cas 1065-31-2

    Cas No: 1065-31-2

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  • Hangzhou Fandachem Co.,Ltd
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1065-31-2 Usage

Description

2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE is a complex organic compound with a unique molecular structure. It is characterized by its benzoquinone core, which is substituted with various functional groups, including two methoxy groups and a farnesylfarnesyl group. 2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE is likely to have specific applications in various fields due to its distinct chemical properties.

Uses

Used in Analytical Chemistry:
2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE is used as an internal standard for liquid-chromatography mass-spectrometry (LC-MS) to ensure accurate quantification of target compounds. Its stability and compatibility with the analytical method make it a suitable choice for this application.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE may be used to study its effect on peroxisome proliferator-activated receptor (PPAR). This could potentially lead to the development of new drugs targeting PPAR, which are involved in various cellular processes, including lipid metabolism and inflammation.
Used in Chromatography:
2,3-DIMETHOXY-5-METHYL-6-[ALL TRANS]FARNESYLFARNESYL-1,4-BENZOQUINONE is also utilized in reversed-phase high pressure liquid chromatography (RP-HPLC) to quantify yeast quinones. Its chemical properties allow for effective separation and quantification of these compounds, which are important for understanding yeast metabolism and its applications in various industries.

Biochem/physiol Actions

Coenzyme Q6 (CoQ6) in the plasma membrane of Saccharomyces cerevisiae is involved in the ascorbate stabilization at the plasma membrane.

Check Digit Verification of cas no

The CAS Registry Mumber 1065-31-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1065-31:
(6*1)+(5*0)+(4*6)+(3*5)+(2*3)+(1*1)=52
52 % 10 = 2
So 1065-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C39H58O4/c1-28(2)16-11-17-29(3)18-12-19-30(4)20-13-21-31(5)22-14-23-32(6)24-15-25-33(7)26-27-35-34(8)36(40)38(42-9)39(43-10)37(35)41/h16,18,20,22,24,26H,11-15,17,19,21,23,25,27H2,1-10H3/b29-18+,30-20+,31-22+,32-24+,33-26+

1065-31-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ubiquinone-6

1.2 Other means of identification

Product number -
Other names CoQ6

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1065-31-2 SDS

1065-31-2Downstream Products

1065-31-2Relevant articles and documents

A convergent approach to coenzyme Q

Lipshutz, Bruce H.,Bulow, Gerd,Fernandez-Lazaro, Fernando,Kim, Sung-Kyu,Lowe, Richard,Mollard, Paul,Stevens, Kirk L.

, p. 11664 - 11673 (2007/10/03)

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.

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