(1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE

Base Information

• Chemical Name: (1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE
• CAS No.: 16934-77-3
• Molecular Formula: C10H21N
• Molecular Weight: 155.283
• Mol file: 16934-77-3.mol

Synonyms:(1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE

Chemical Property of (1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE

Chemical Property:

• Boiling Point: 192.8±8.0 °C(Predicted)
• PKA: 10.68±0.70(Predicted)
• PSA: 26.02000
• Density: 0.834±0.06 g/cm3(Predicted)
• LogP: 3.10620
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C

Purity/Quality:

97% ^*data from raw suppliers

(1R,2R,5R)-2-Isopropyl-5-methylcyclohexanamine 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE

There total 19 articles about (1R,2R,5R)-2-ISOPROPYL-5-METHYLCYCLOHEXANAMINE 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: 98.0%

DL-neomenthol (490-99-3,491-01-0,491-02-1,1490-04-6,2216-51-5,2216-52-6,3623-51-6,3623-52-7,3623-53-8,15356-60-2,15356-70-4,20747-49-3,20752-33-4,20752-34-5,23283-97-8,64282-88-8,89-78-1) → rac-menthylamine (2216-54-8,4894-99-9,7231-40-5,16934-77-3,20706-69-8,20706-70-1,21411-81-4,23399-21-5,51743-63-6,66609-74-3,85549-06-0,787534-09-2)

Guidance literature:

DL-neomenthol; With 1-methyl-1H-imidazole; methanesulfonyl chloride; triethylamine; In toluene; at 20 ℃; for 2h;

With sodium azide; In N,N-dimethyl-formamide; at 40 ℃; for 48h;

With hydrogen; nickel; In tetrahydrofuran; at 20 ℃; for 72h;

DOI:10.1002/ejoc.201301566

Reference yield: 98.0%

2‐azido‐1‐isopropyl‐4‐methylcyclohexane (898543-45-8,898543-46-9) → rac-menthylamine (2216-54-8,4894-99-9,7231-40-5,16934-77-3,20706-69-8,20706-70-1,21411-81-4,23399-21-5,51743-63-6,66609-74-3,85549-06-0,787534-09-2)

Guidance literature:

With hydrogen; In tetrahydrofuran; at 20 ℃; for 72h;

DOI:10.1055/s-0030-1258295

Reference yield:

(1R,5S)-menthone oxime (65620-72-6,165874-36-2) → (2R,5S)-menthone (10458-14-7,14073-97-3,17627-49-5,7786-64-3) + Neoisomenthylamine (16934-77-3,787534-09-2) + L-menthylamine (2216-54-8,787534-09-2) + (+)-(1R,3S,4S)-neomenthylamine (7231-40-5,787534-09-2) + isomenthylamine (160399-90-6,787534-09-2) + (1R,4R)-(+)-isomenthone (1196-31-2,17627-49-5,7786-64-3)

Guidance literature:

With hydrogen; In toluene; at 100 ℃; under 5625.56 Torr;

DOI:10.1016/j.apcata.2020.117799

upstream raw materials:

(2R,5S)-menthone

ammonium formate

(+)-isomenthone oxime

(R)-Citronellal

Downstream raw materials:

N-((1R)-neoisomenthyl)-isobutyramide

(+)-(1R,3S,4S)-neomenthylamine

(+)-neomenthylamine

2-isopropyl-5-methyl-cyclohexylamine

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