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619-68-1

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619-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 619-68-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 619-68:
(5*6)+(4*1)+(3*9)+(2*6)+(1*8)=81
81 % 10 = 1
So 619-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NO3/c9-7(10)5-1-3-6(8-11)4-2-5/h1-4H,(H,9,10)

619-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrosobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 4-nitroso-

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:619-68-1 SDS

619-68-1Relevant articles and documents

Naked-eye bead property estimation using a red safety-catch linker

Heidler, Philipp,Link, Andreas

, p. 182 - 187 (2005)

The attachment of linker molecules to polymer beads used as insoluble supports for organic synthesis is a frequent requirement. Defined immobilization of these tinker molecules before loading selected building blocks is crucial for subsequent transformati

Transketolase Catalyzed Synthesis of N-Aryl Hydroxamic Acids

Fúster Fernández, Inés,Hecquet, Laurence,Fessner, Wolf-Dieter

, p. 612 - 621 (2021/12/08)

Hydroxamic acids are metal-chelating compounds that show important biological activity including anti-tumor effects. We have recently engineered the transketolase from Geobacillus stearothermopilus (TKgst) to convert benzaldehyde as a non-natur

Photochromic Evaluation of 3(5)-Arylazo-1 H-pyrazoles

Rustler, Karin,Nitschke, Philipp,Zahnbrecher, Sophie,Zach, Julia,Crespi, Stefano,K?nig, Burkhard

, p. 4079 - 4088 (2020/04/09)

The desire to photocontrol molecular properties ranging from materials to pharmacology using light as an external trigger with high spatiotemporal resolution led to the development of a broad range of photochromic scaffolds. Among them, azobenzenes are synthetically well accessible and show excellent fatigue resistance. Their photochromic properties vary with the substitution pattern and for different heteroarenes. However, the photochromism of 3(5)-substituted-1H-pryazoles has not yet been investigated, although this compound class offers interesting possibilities of metal ion coordination and hydrogen bond formation via its NH moiety. Herein, we present the results of an experimental and computational investigation of arylazo-3(5)-arylazo-1H-pyrazoles. To elucidate their properties, solvent and substitution effects on their light absorption, thermal half-lives, photostationary states, fatigue, and quantum yields were determined.

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