(1S,2R)-2-methylcyclohexanamine hydrochloride

Base Information

• Chemical Name: (1S,2R)-2-methylcyclohexanamine hydrochloride
• CAS No.: 79389-39-2
• Molecular Formula: C7H15N.HCl
• Molecular Weight: 149.664
• Hs Code.: 2921309990
• Mol file: 79389-39-2.mol

Synonyms:(1S,2R)-2-methylcyclohexanamine hydrochloride;(1S,2R)-2-Methyl-cyclohexylamine hydrochloride;cis-2-Methyl-cyclohexylamine hydrochloride

Chemical Property of (1S,2R)-2-methylcyclohexanamine hydrochloride

Chemical Property:

• PSA: 26.02000
• LogP: 3.02610
• Storage Temp.: Inert atmosphere,Room Temperature

Purity/Quality:

97% ^*data from raw suppliers

(1S,2R)-2-Methylcyclohexylamine hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (1S,2R)-2-methylcyclohexanamine hydrochloride

There total 18 articles about (1S,2R)-2-methylcyclohexanamine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 65.5%

(αS,1S,2R)-(-)-cis-2-Methyl-N-(1-phenylethyl)cyclohexanamin-hydrochlorid (91603-26-8) → (1S,2R)-(-)-cis-2-Methyl-cyclohexanamin-hydrochlorid (79389-39-2)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethanol; for 24h; under 2585.81 Torr;

Reference yield: 61.0%

→ trans-2-methyl-1-cyclohexanamine hydrochloride (10049-61-3,39558-31-1,79265-66-0,79389-39-2,79389-41-6,91603-44-0,91603-46-2,104485-19-0)

Guidance literature:

Reference yield: 37.0%

(2-methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine → (1S,2R)-(-)-cis-2-Methyl-cyclohexanamin-hydrochlorid (79389-39-2)

Guidance literature:

(2-methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; With hydrogen; 20% Pd(OH)2/C; In ethanol; at 20 ℃; under 760.051 Torr;

With hydrogenchloride; In 1,4-dioxane; dichloromethane;

upstream raw materials:

((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride

((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride

E/Z-<2(RS)>-2-Methyl-N-(R-α-methylbenzyl)-cyclohexaneimine

E/Z-<2(RS)>-2-Methyl-N-(S-α-methylbenzyl)-cyclohexaneimine

Downstream raw materials:

(S)-3-Benzyloxycarbonylamino-N-[(R)-1-((1S,2R)-2-methyl-cyclohexylcarbamoyl)-ethyl]-succinamic acid benzyl ester

6-amino-4-((1S,2R)-2-methylcyclohexylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide

4-((1S,2R)-2-methylcyclohexylamino)-6-nitropyrrolo[1,2-b]pyridazine-3-carboxamide

4-((1S,2R)-2-methylcyclohexylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide

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