606974-29-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is an alternative name for the compound, which is used to describe its structure and composition.
Explanation
Diamines are a group of organic compounds that contain two amino groups, which is the defining characteristic of 1,2-Butanediamine,N,N,N,N,3-pentamethyl-,(2S)-(9CI).
Explanation
The compound is in a liquid state at room temperature and is colorless in appearance.
Explanation
The compound has a distinct smell that is similar to ammonia.
Explanation
The compound can dissolve in water, which is an important property for its various applications.
Explanation
These are some of the main uses of the compound in various industries.
Explanation
The compound should be handled with care due to its flammability and potential health risks if it comes into contact with the respiratory system or is ingested.
Class
Diamines
Physical state
Colorless liquid
Odor
Strong ammonia-like
Solubility
Soluble in water
Industrial applications
a. Corrosion inhibitor in the petroleum industry
b. Curing agent in epoxy resins
c. Production of pharmaceuticals and agricultural chemicals
Safety precautions
Flammable liquid, harmful if inhaled or ingested
Check Digit Verification of cas no
The CAS Registry Mumber 606974-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,6,9,7 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 606974-29:
(8*6)+(7*0)+(6*6)+(5*9)+(4*7)+(3*4)+(2*2)+(1*9)=182
182 % 10 = 2
So 606974-29-2 is a valid CAS Registry Number.
606974-29-2Relevant academic research and scientific papers
Coldham, Iain,O'Brien, Peter,Patel, Jignesh J.,Raimbault, Sophie,Sanderson, Adam J.,Stead, Darren,Whittaker, David T.E.
, p. 2113 - 2119 (2007)
A selection of chiral ligands was screened for the asymmetric deprotonation of N-Boc-piperidine. The asymmetric deprotonation of this compound is notoriously difficult and reasonable yields are obtained only with non-hindered ligands, such as tetramethyle
Asymmetric catalysis. Part 153: Metal-catalysed enantioselective α-ketol rearrangement
Brunner, Henri,Kagan, Henri B.,Kreutzer, Georg
, p. 2177 - 2187 (2007/10/03)
Promoted by catalytic amounts of Ni complexes tertiary α-hydroxyketones 1a, 3a-5a undergo rearrangement, forming chiral isomers 1b, 3b-5b. The best enantioselection was obtained with the model system 1-benzoylcyclopentanol 4a/2-hydroxy-2-phenylcyclohexanone 4b. In a ligand screening 2-[4-(S)-tert-butyloxazolin-2-yl]pyridine gave the highest enantiomeric excess of 46% (S)-4b. The analogous isomerisation reactions of α-hydroxyimines 6a, 7a forming chiral α-aminoketones 6b, 7b were established.
