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114853-42-8

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114853-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114853-42-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,5 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114853-42:
(8*1)+(7*1)+(6*4)+(5*8)+(4*5)+(3*3)+(2*4)+(1*2)=118
118 % 10 = 8
So 114853-42-8 is a valid CAS Registry Number.

114853-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Dioxo-1,2,5,6-tetrahydro-4H-benzo[g]imidazo[1,2,3-ij]pteridin -12-ium chloride

1.2 Other means of identification

Product number -
Other names -

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:114853-42-8 SDS

114853-42-8Downstream Products

114853-42-8Relevant articles and documents

Regulating Cofactor Balance In Vivo with a Synthetic Flavin Analogue

Tan, Zhuotao,Zhu, Chenjie,Fu, Jingwen,Zhang, Xiaowang,Li, Ming,Zhuang, Wei,Ying, Hanjie

supporting information, p. 16464 - 16468 (2018/11/23)

A novel strategy to regulate cofactor balance in vivo for whole-cell biotransformation using a synthetic flavin analogue is reported. High efficiency, easy operation, and good applicability were observed for this system. Confocal laser scanning microscopy was employed to verify that the synthetic flavin analogue can directly permeate into Escherichia coli cells without modifying the cell membrane. This work provides a promising intracellular redox regulatory approach to construct more efficient cell factories.

Chemoselective sulfide oxidation mediated by bridged flavinium organocatalysts

Marsh, Barrie J.,Carbery, David R.

scheme or table, p. 2362 - 2365 (2010/05/19)

The chemoselective oxidation of sulfides to sulfoxides, catalysed by bridged, tetracyclic flavinium catalysts is presented. The flavinium catalysts are easily prepared via a telescoped three-step process. A range of sulfoxides is accessed in excellent yield and chemoselectivity.

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