MN-25

Base Information

Chemical Name:MN-25
CAS No.:501927-29-3
Molecular Formula:C27H39N3O3
Molecular Weight:453.625
Hs Code.:
Mol file:501927-29-3.mol

Synonyms:7-Methoxy-2-methyl-1-[2-(4-morpholinyl)ethyl]-N-[(1S,2S,4R)-1,3,3 -trimethylbicyclo[2.2.1]hept-2-yl]-1H-indole-3-carboxamide;

Suppliers and Price of MN-25

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Cayman Chemical
MN-25-2-methyl derivative ≥95%
10mg
$ 562.00

Cayman Chemical
MN-25-2-methyl derivative ≥95%
5mg
$ 317.00

Cayman Chemical
MN-25-2-methyl derivative ≥95%
1mg
$ 71.00

AK Scientific
7-Methoxy-2-methyl-1-(2-morpholin-4-ylethyl)-N-[(1S,2S,4R)-1,3,3-trimethyl-2-bicyclo[2.2.1]heptanyl]indole-3-carboxamide
10mg
$ 802.00

AK Scientific
7-Methoxy-2-methyl-1-(2-morpholin-4-ylethyl)-N-[(1S,2S,4R)-1,3,3-trimethyl-2-bicyclo[2.2.1]heptanyl]indole-3-carboxamide
1mg
$ 187.00

Total 23 raw suppliers

Chemical Property of MN-25

Chemical Property:

PSA：59.22000
LogP:4.74780

Purity/Quality:

99% ^*data from raw suppliers

MN-25-2-methyl derivative ≥95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description MN-25-2-methyl derivative is a cannabinoid (CB) receptor ligand with Ki values of 8 and 29 nM at the central CB1 receptor and peripheral CB2 receptor, respectively. This product is intended for forensic and research applications.
Uses MN-25, is a synthetic cannabinoid (CB) with greater affinity for the peripheral CB2 receptor (Ki = 11 nM) than for the central CB1 receptor (Ki = 245 nM). Synthetic Cannabinoids

Technology Process of MN-25

There total 6 articles about MN-25 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:

: 53512-46-2
2-methyl-7-methoxy indole

: 501927-29-3
7-methoxy-2-methyl-1-[2-(4-morpholinyl)ethyl]-N-[(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept2-yl]-1H-indole-3-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: collidine / acetonitrile

2: KOH

3: NaH / dimethylformamide

4: 3 N aq. NaOH / methanol

5: SOCl₂ / 1,2-dichloro-ethane

6: TEA / 1,2-dichloro-ethane

With 2,3,5-trimethyl-pyridine; potassium hydroxide; sodium hydroxide; thionyl chloride; TEA; sodium hydride; In methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0960-894X(02)00466-3

Reference yield:

: 354573-92-5
methyl 7-methoxy-2-methyl-1H-indole-3-carboxylate

: 501927-29-3
7-methoxy-2-methyl-1-[2-(4-morpholinyl)ethyl]-N-[(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept2-yl]-1H-indole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / dimethylformamide

2: 3 N aq. NaOH / methanol

3: SOCl₂ / 1,2-dichloro-ethane

4: TEA / 1,2-dichloro-ethane

With sodium hydroxide; thionyl chloride; TEA; sodium hydride; In methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00466-3

Reference yield:

: 354573-93-6
2-methyl-3-trichloroacetyl-7-methoxyindole

: 501927-29-3
7-methoxy-2-methyl-1-[2-(4-morpholinyl)ethyl]-N-[(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept2-yl]-1H-indole-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: KOH

2: NaH / dimethylformamide

3: 3 N aq. NaOH / methanol

4: SOCl₂ / 1,2-dichloro-ethane

5: TEA / 1,2-dichloro-ethane

With potassium hydroxide; sodium hydroxide; thionyl chloride; TEA; sodium hydride; In methanol; 1,2-dichloro-ethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00466-3