6051-30-5 Usage
Diamide derivative
of butane-1,2,3-triol 2,3-Dihydroxybutanediamide is derived from butane-1,2,3-triol by replacing two hydroxyl groups with amide groups.
Classification
Chelating agent, specifically a polyamine It is a compound that can form complexes with metal ions, and it belongs to the class of polyamine chelating agents.
Common use
Component of lysis buffer It is used in biochemistry and molecular biology to help extract proteins and nucleic acids.
Potential therapeutic applications
Treatment of cancer and neurodegenerative diseases Research is being conducted on its possible use in treating certain diseases.
Use in analytical chemistry
Chiral resolving agent for enantiomer separation It helps in separating different forms of chiral compounds, called enantiomers, in analytical processes.
Applications
Research, medical, and industrial settings Due to its chelating and protein-binding properties, 2,3-Dihydroxybutanediamide is used in various fields, including research, medicine, and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 6051-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6051-30:
(6*6)+(5*0)+(4*5)+(3*1)+(2*3)+(1*0)=65
65 % 10 = 5
So 6051-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O4/c5-3(9)1(7)2(8)4(6)10/h1-2,7-8H,(H2,5,9)(H2,6,10)
6051-30-5Relevant articles and documents
From single molecule to crystal: Mapping out the conformations of tartaric acids and their derivatives
Janiak, Agnieszka,Rychlewska, Urszula,Kwit, Marcin,Stepien, Urszula,Gawronska, Krystyna,Gawronski, Jacek
experimental part, p. 1500 - 1506 (2012/07/28)
Stereoisomers of one of the most important organic compounds, tartaric acid, optically active and meso as well as the ester or amide derivatives, can show diverse structures related to the rotation around the three carbon-carbon bonds. This study determin
