40015-92-7 Usage
Uses
Used in Chemical Synthesis:
2-(Aminomethyl)cyclohexanamine is used as an intermediate in the chemical synthesis for the production of pharmaceuticals, pesticides, and rubber chemicals. Its cyclohexane ring and amine functional group provide a versatile platform for the creation of a variety of compounds.
Used in Corrosion Inhibition:
In the industry, 2-(Aminomethyl)cyclohexanamine is used as a corrosion inhibitor to protect metal surfaces from degradation, thereby extending the lifespan of equipment and structures.
Used in Epoxy Resin Systems:
2-(Aminomethyl)cyclohexanamine is used as a curing agent in epoxy resin systems, enhancing the properties of the final product, such as its hardness and durability.
Used in Stabilization of Organic Peroxides:
As a stabilizer for organic peroxides, 2-(Aminomethyl)cyclohexanamine helps to control the decomposition rate of these compounds, which is crucial in various chemical processes and applications.
Used in Safety Measures:
Due to its potential to cause irritation and harmful effects at high concentrations, 2-(Aminomethyl)cyclohexanamine is also used as a reminder of the importance of proper safety measures during its handling and use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40015-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40015-92:
(7*4)+(6*0)+(5*0)+(4*1)+(3*5)+(2*9)+(1*2)=67
67 % 10 = 7
So 40015-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2/c8-5-6-3-1-2-4-7(6)9/h6-7H,1-5,8-9H2
40015-92-7Relevant academic research and scientific papers
EXPERIMENTAL STUDIES OF THE ANOMERIC EFFECT. PART 2 RING INVERSION AND NITROGEN INVERSION EQUILIBRIA IN CIS-DECAHYDROQUINAZOLINES
Booth, Harold,Khedhair, Khedhair A.,Al-Shirayda, Hatif A. R. Y.
, p. 1465 - 1476 (2007/10/02)
The positions of conformational equilibria due to the double ring inversion in cis-decahydroquinazoline (7-->//07-->8 1.08 kcal mol-1; -ΔG09-->10 1.10 kcal mol-1) for the conformation which would allow the lone pairs on N(1) and N(3) to lie on the hindered 'inside' face of the molecules.However, the values of 3J(CHNH) coupling constants for both cis-decahydro-3-methylquinazoline (10) and cis (4aH, 8aH) cis (2H, 8aH)-decahydro-2,3-dimethylquinazoline (14) show that the N-inversion equilibrium at N(1) prefers the conformation in which N(1)-H is 'inside' (axial), and N(1)-lone pair equatorial, thus demonstrating the ability of the anomeric effect to outweigh steric repulsions.
