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Ubiquinone Q2, also known as Coenzyme Q2, is a naturally occurring chemical compound that plays a crucial role in cellular energy production. It is a member of the ubiquinone family, which are essential components of the electron transport chain in mitochondria, facilitating the conversion of nutrients into ATP, the primary energy currency of cells. Q2 is particularly important in the process of oxidative phosphorylation, where it helps transfer electrons and protons, thus contributing to the generation of a proton gradient that powers ATP synthesis. While it is structurally similar to the more widely known Ubiquinone Q10, Q2 has a shorter isoprenoid tail, which may affect its bioavailability and function in the body. Research on Q2 is ongoing, but it is believed to have potential implications for energy metabolism and may be of interest in the context of certain health conditions and aging.

7704-04-3

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7704-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7704-04-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7704-04:
(6*7)+(5*7)+(4*0)+(3*4)+(2*0)+(1*4)=93
93 % 10 = 3
So 7704-04-3 is a valid CAS Registry Number.

7704-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-geranyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone

1.2 Other means of identification

Product number -
Other names 2-((E)-3,7-Dimethyl-octa-2,6-dienyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone

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:7704-04-3 SDS

7704-04-3Downstream Products

7704-04-3Relevant academic research and scientific papers

A new synthetic route to substituted quinones by radical-mediated coupling of organotellurium compounds with quinones

Yamago, Shigeru,Hashidume, Masahiro,Yoshida, Jun-Ichi

, p. 6805 - 6813 (2007/10/03)

Carbon-centered radicals generated from the corresponding organotellurium compounds react with a variety of quinones under photo-thermal conditions to give the monoaddition product in moderate to excellent yield. The reaction can be used for the synthesis of polyprenyl quinoid natural products and C-glycosides.

Radical-mediated synthesis of substituted quinones with organotellurium compounds

Yamago, Shigeru,Hashidume, Masahiro,Yoshida, Jun-Ichi

, p. 1234 - 1235 (2007/10/03)

Carbon-centered radicals generated from the corresponding organotellurium compounds react with a variety of quinones under photo-thermal conditions to give the monoaddition product in good to excellent yield. The reaction can be used for the synthesis of polyprenyl quinoid natural products.

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