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flavin mononucleotide semiquinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34469-63-1

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34469-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34469-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,6 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34469-63:
(7*3)+(6*4)+(5*4)+(4*6)+(3*9)+(2*6)+(1*3)=131
131 % 10 = 1
So 34469-63-1 is a valid CAS Registry Number.

34469-63-1SDS

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 [(2S,3R,4R)-5-(7,8-dimethyl-2,4-dioxobenzo[g]pteridin-10-yl)-2,3,4-trihydroxypentyl] dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names EINECS 205-664-7

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:34469-63-1 SDS

34469-63-1Relevant academic research and scientific papers

Site-Selective Synthesis of 15N- and 13C-Enriched Flavin Mononucleotide Coenzyme Isotopologues

Neti, Syam Sundar,Poulter, C. Dale

, p. 5087 - 5092 (2016/07/06)

Flavin mononucleotide (FMN) is a coenzyme for numerous proteins involved in key cellular and physiological processes. Isotopically labeled flavin is a powerful tool for studying the structure and mechanism of flavoenzyme-catalyzed reactions by a variety of techniques, including NMR, IR, Raman, and mass spectrometry. In this report, we describe the preparation of labeled FMN isotopologues enriched with 15N and 13C isotopes at various sites in the pyrazine and pyrimidine rings of the isoalloxazine core of the cofactor from readily available precursors by a five-step chemo-enzymatic synthesis.

Preparation of riboflavin 5'-phosphate (FMN) and its sodium salt in a lactone

-

, (2008/06/13)

An improved process for preparing riboflavin 5'-phosphate (FMN) or its monosodium salt by reacting riboflavin with excess phosphorus oxychloride in a solvent, hydrolyzing of the resulting reaction mixture and, if desired, partially neutralizing with aqueous sodium hydroxide solution, comprises reacting the riboflavin with from 1.2 to 3 moles of phosphorus oxychloride per mole of riboflavin in a suitable lactone, especially γ-butyrolactone, as solvent. The process is particularly advantageous when the reaction mixture is hydrolyzed at from 80° to 90° C. continuously or batchwise.

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