6163-56-0 Usage
Explanation
The compound consists of 5 carbon atoms, 11 hydrogen atoms, and 1 nitrogen atom in its molecular structure.
Explanation
It is an amine compound because it contains a nitrogen atom bonded to carbon atoms and has two methyl groups attached to the nitrogen atom.
3. Propenyl group present
Explanation
The compound contains a propenyl group (a vinyl group) with a double bond between two carbon atoms and one hydrogen atom.
4. N,N-dimethyl substitution
Explanation
Two methyl groups are attached to the nitrogen atom, which influences the compound's reactivity and physical properties.
Explanation
1-Propen-1-amine, N,N-dimethylis often used as an intermediate in the synthesis of various chemicals and pharmaceuticals due to its reactive nature.
Explanation
The compound is used in the production of polymers, contributing to the formation of large molecules with repeating structural units.
Explanation
1-Propen-1-amine, N,N-dimethylacts as a cross-linking agent in some industrial processes, helping to create a network of linked polymer chains.
Explanation
This chemical should be handled with caution as it can be toxic if ingested or inhaled and corrosive to the skin and eyes upon contact.
Chemical class
Amine
Common use
Intermediate in chemical synthesis
Application
Polymer production
Industrial use
Cross-linking agent
Safety concerns
Toxicity and corrosiveness
Check Digit Verification of cas no
The CAS Registry Mumber 6163-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6163-56:
(6*6)+(5*1)+(4*6)+(3*3)+(2*5)+(1*6)=90
90 % 10 = 0
So 6163-56-0 is a valid CAS Registry Number.
6163-56-0Relevant articles and documents
Gas-Phase Elimination Kinetics of (Dimethylamino)alkyl Acetates. The Ion-Pair Mechanism through Neighboring Group Participation.
Chuchani, Gabriel,Rotinov, Alexandra,Dominguez, Rosa M.,Gonzalez, Neil
, p. 4157 - 4160 (2007/10/02)
The gas-phase elimination kinetics of some amino esters and a keto acetate have been studied in the temperature region of 260.0-411.5 deg C and in the pressure range of 21.5-170.0 torr.These eliminations, in vessels seasoned with allyl bromide, are predominantly unimolecular and homogenous and obey a first order rate law.The rate coefficients for the reactions are expressible by the following Arrhenius equations: for 3-(dimethylamino)-1-propyl acetate (1), log k1 (s-1) = (12.97 +/- 0.20) - (202.1 +/- 2.5) kJ mol-1 (2.303RT)-1; for 4-(dimethylamino)-1-butyl acetate (4), log k1 (s-1) = (11.91 +/- 0.43) - (163.5 +/- 4.8) kJ mol-1 (2.303 RT)-1; for 4-oxo-1-pentyl acetate (7), log k1 (s-1) = (12.77 +/- 0.36) - (202.8 +/- 4.6) kJ mol-1 (2.303RT)-1.The presence of the (CH3)2N group in these acetates appears to provide anchimeric assistance in the elimination; methyl acetate and the corresponding heterocyclic products arise from an intimate ion-pair mechanism.The CH3CO substituent is believed to influence the pyrolysis rate of 5-acetoxy-2-pentanone by a weak steric acceleration.
