40015-92-7 Usage
General Description
2-(Aminomethyl)cyclohexanamine, also known as AMCHA, is a chemical compound with a cyclohexane ring structure and an amine functional group. It is a colorless to light yellow liquid with a strong ammonia-like odor. AMCHA is used in various industrial applications, including as a corrosion inhibitor and as an intermediate in the production of pharmaceuticals, pesticides, and rubber chemicals. It is also used as a curing agent in epoxy resin systems and as a stabilizer for organic peroxides. AMCHA is considered to have low toxicity, but exposure to high concentrations can cause irritation to the eyes, skin, and respiratory system, and may have harmful effects on the central nervous system and kidneys. Therefore, proper safety measures should be followed when handling this chemical.
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 articles and documents
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.
