31329-52-9 Usage
Functional groups
Two amino groups (-NH2)
Two hydroxyethyl groups (-CH2CH2OH)
Chemical structure
A 1,2-ethanediamine backbone with two aminoethyl chains and two hydroxyethyl chains attached to the nitrogen atoms
Physical state
Likely a liquid or a low melting point solid due to the presence of multiple amine and ether groups
Solubility
Soluble in water and polar organic solvents due to its polar nature
Chelating agent
Forms stable complexes with metal ions
Corrosion inhibitor
Prevents or slows down the corrosion of metals
Pharmaceutical production
Used in the synthesis of various drugs
Pesticide production
Used in the synthesis of agrochemicals
Dye production
Used in the synthesis of dyes
Synthesis of complex organic molecules
Acts as a building block for various organic compounds
Polymer and resin production
Used as a monomer or building block for polymers and resins
Precursors
Important precursor for the synthesis of various pharmaceutical drugs and agrochemicals
Reactivity
Can undergo reactions with electrophiles due to the presence of nucleophilic amine and ether groups
Can form hydrogen bonds with other molecules, contributing to its solubility in water and polar solvents
Safety
Potential health hazards due to its amine and ether groups, and should be handled with care and proper safety measures
Check Digit Verification of cas no
The CAS Registry Mumber 31329-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,2 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31329-52:
(7*3)+(6*1)+(5*3)+(4*2)+(3*9)+(2*5)+(1*2)=89
89 % 10 = 9
So 31329-52-9 is a valid CAS Registry Number.
31329-52-9Relevant articles and documents
NUCLEOPHILIC CLEAVAGE AND FORMATION OF SATURATED HETEROCYCLES. IX. KINETICS OF THE AMINATION OF 1-AZIRIDINE
Bobylev, V. A.,Dalin, A. R.,Borisenko, I. V.,Kamskaya, O. I.
, p. 1003 - 1007 (2007/10/02)
1.Enlarging the aminoethyl substituent at the heteroatom of the aziridine ring results in a decrease in reactivity and an increase in substrate selectivity towards nucleophilic cleavage by amines. 2.The reactivity of amines in the nucleophilic cleavage of 1-aziridine is largely governed by the steric accessibility of the nitrogen atoms of the nucleophile.Amino groups in which the environment of the reaction site is the same have similar reactivities.
