755711-20-7 Usage
Structure
Cyclohexane ring with two amine groups and a methyl group
The molecule has a six-membered carbon ring (cyclohexane) with two nitrogen atoms (amine groups) attached at the 1st and 2nd positions, and a methyl group (CH3) attached at the 3rd position.
Chirality
Chiral molecule
The molecule has a specific stereochemistry, meaning it has a non-superimposable mirror image (enantiomer).
Stereochemistry
[1S-(1alpha,2alpha,3alpha)]
The stereochemistry of the molecule is designated as [1S-(1alpha,2alpha,3alpha)], which indicates the spatial arrangement of the atoms in the molecule.
Derivative
1,2-Cyclohexanediamine
The compound is a derivative of 1,2-Cyclohexanediamine, with a methyl group added to the third position of the carbon ring.
Applications
Organic synthesis, pharmaceuticals, agrochemicals
The compound is used as a building block in organic synthesis for creating various pharmaceutical and agrochemical products.
Potential Applications
Medicinal chemistry, drug development, polymer production
Due to its unique chemical structure, the compound may have potential applications in the fields of medicinal chemistry and drug development, as well as industrial uses in the production of polymers and other materials.
Check Digit Verification of cas no
The CAS Registry Mumber 755711-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,5,7,1 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 755711-20:
(8*7)+(7*5)+(6*5)+(5*7)+(4*1)+(3*1)+(2*2)+(1*0)=167
167 % 10 = 7
So 755711-20-7 is a valid CAS Registry Number.
755711-20-7Relevant academic research and scientific papers
METHOD FOR PRODUCING 1,2-DIAMINO-3-METHYLCYCLOHEXANE AND/OR 1,2-DIAMINO-4-METHYLCYCLOHEXANE
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Page/Page column 5-7, (2008/06/13)
The invention relates to a method for producing 1,2-diamino-3-methylcyclohexane and/or 1,2-diamino-4-methylcyclohexane by reacting 2,3- and/or 3,4-diaminotoluol with hydrogen under high pressure and high temperature in the presence of a heterogene catalys
Studies of the Metal Complexes of Cyclohexane Derivatives. VIII. Preparation and Properties of Platinum(II) and Cobalt(III) Complexes Containing (1R,2S,3S)- or (1S,2R,3R)-3-methyl-1,2-cyclohexanediamine
Saito, Reiko,Kidani, Yoshinori
, p. 3430 - 3436 (2007/10/02)
(1RS,2SR,3SR)-3-Methyl-1,2-cyclohexanediamine (3m-chxn), a methyl derivative of cis-1,2-cyclohexanediamine, was prepared and optically resolved.The absolute configurations of the enantiomers obtained were assigned on the basis of the Cotton effect of the trans-dichlorobis(diamine) complexes, each containing active 3m-chxn.The complexes of the 3)2L>2+, 2+, and 3>3+ types (en=1,2-ethanediamine, L=R,S,S- or S,R,R-3m-chxn) were also synthesized and characterized on the basis of their absorption, CD, and 13C NMR spectra.It has been found that the chelate rings adopted by R,S,S- and S,R,R-3m-chxn predominantly take δ and λ conformations respectively, because of the preferred equatorial orientation of the C2-C3 bond of the cyclohexane ring.The four diastereomers of 3>3+ were chromatographically isolated and assigned to fac-Λ(lel3), mer-Λ(lel3), fac-Δ(ob3), and mer-Δ(ob3).
