(S)-Methocarbamol

Base Information

Chemical Name:(S)-Methocarbamol
CAS No.:108914-10-9
Molecular Formula:C₁₁H₁₅NO₅
Molecular Weight:241.244
Hs Code.:
Mol file:108914-10-9.mol

Synonyms:1,2-Propanediol,3-(2-methoxyphenoxy)-, 1-carbamate, (S)-; Carbamic acid,(-)-2-hydroxy-3-(o-methoxyphenoxy)propyl ester (7CI); (S)-Methocarbamol

Suppliers and Price of (S)-Methocarbamol

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

TRC
(S)-Methocarbamol
25mg
$ 165.00

Medical Isotopes, Inc.
(S)-Methocarbamol
250 mg
$ 2200.00

Medical Isotopes, Inc.
(S)-Methocarbamol
25 mg
$ 650.00

Total 1 raw suppliers

Chemical Property of (S)-Methocarbamol

Chemical Property:

Purity/Quality:: (S)-Methocarbamol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

General Description (S)-Methocarbamol is a chiral muscle relaxant that can be synthesized enantioselectively from (S)-guaifenesin, as demonstrated in studies exploring its preparation via L-proline-catalyzed α-aminoxylation or resolution methods. Its enantiopure form is of interest due to its pharmacological activity, though the specific stereochemical effects on its efficacy or metabolism are not detailed in the provided abstracts.

Technology Process of (S)-Methocarbamol

There total 19 articles about (S)-Methocarbamol 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: 95.0%

: 2049-21-0
rac-4-(2-methoxyphenoxymethyl)-[1,3]dioxolan-2-one

: 532-03-6,108914-10-9,145841-69-6
methocarbamol

Guidance literature:: With ammonium hydroxide; at 40 ℃; for 6h;

Reference yield: 89.0%

: (R)-4-((2-methoxyphenoxy)methyl)-1,3-dioxolan-2-one

: 108914-10-9,145841-69-6
(R)-1-carbamoyloxy-2-hydroxy-3-(2-methoxyphenoxy)propane

Guidance literature:: With ammonia; In isopropyl alcohol; for 12h;
DOI:10.1080/00397911.2010.493631

Reference yield:

: 93950-95-9
1-benzyloxy-2-carbamoyloxy-3-(2-methoxy-phenoxy)-propane

: 532-03-6,108914-10-9,145841-69-6
methocarbamol

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd-C

2: aq. NH₃

With ammonium hydroxide; hydrogen; palladium on activated charcoal;
DOI:10.1007/BF00900262