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52590-98-4

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52590-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52590-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,9 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52590-98:
(7*5)+(6*2)+(5*5)+(4*9)+(3*0)+(2*9)+(1*8)=134
134 % 10 = 4
So 52590-98-4 is a valid CAS Registry Number.

52590-98-4SDS

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 ubiquinol 1

1.2 Other means of identification

Product number -
Other names ubiquinol-1

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:52590-98-4 SDS

52590-98-4Relevant articles and documents

Calcium binding and transport by coenzyme Q

Bogeski, Ivan,Gulaboski, Rubin,Kappl, Reinhard,Mirceski, Valentin,Stefova, Marina,Petreska, Jasmina,Hoth, Markus

, p. 9293 - 9303 (2011)

Coenzyme Q10 (CoQ10) is one of the essential components of the mitochondrial electron-transport chain (ETC) with the primary function to transfer electrons along and protons across the inner mitochondrial membrane (IMM). The concomitant proton gradient ac

Synthetic studies on coenzyme Q10: Part 2 - A efficient and improved synthesis of coenzyme Q10 via the C5 + C 45 approach

Dai, Hui-Fang,Chen, Fen-Er,Yu, Xiong-Jie

, p. 1317 - 1321 (2007/10/03)

An improved route to coenzyme Q10 (1) starting from commercially available coenzyme Q1 is described. The key steps in this synthesis are the SeO2-mediated oxidation of the protected isoprenylhydroquinone 3 into the (E)-allyl alcohol 5 without the formation of undesired stereoisomer and the one-pot reductive elimination of the phenylsulfonyl and dibenzyl groups in 7 by using naphthalenyllithium.

Ubiquinone-1

Naruta, Yoshinori,Maruyama, Kazuhiro

, p. 125 - 125 (2017/06/01)

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