l-methylcysteine hydrochloride

Base Information

Chemical Name:l-methylcysteine hydrochloride
CAS No.:403804-61-5
Molecular Formula:C4H9NO2S.ClH
Molecular Weight:171.64600
Hs Code.:
Mol file:403804-61-5.mol

Synonyms:Cysteine, N-methyl-, hydrochloride (9CI);

Suppliers and Price of l-methylcysteine hydrochloride

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

Matrix Scientific
3-Mercapto-2-(methylamino)-propanoic acid hydrochloride 97%
1g
$ 730.00

Advanced Chemicals Intermediatesced Chemicals Intermediates
3-Mercapto-2-methylamino-propionicacid;hydrochloride 95%+
1g
$ 116.00

Acints
3-Mercapto-2-methylamino-propionicacid;hydrochloride 95%+
10g
$ 739.50

Total 3 raw suppliers

Chemical Property of l-methylcysteine hydrochloride

Chemical Property:

PSA：88.13000
LogP:0.78170

Purity/Quality:

98% ^*data from raw suppliers

3-Mercapto-2-(methylamino)-propanoic acid hydrochloride 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of l-methylcysteine hydrochloride

There total 1 articles about l-methylcysteine 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: 66.0%

: 34592-47-7,2756-91-4,6070-92-4,60731-25-1
L-thioproline

: 14344-46-8,403804-61-5
(R)-N-methylcysteine hydrochloride

Guidance literature:: With ammonium chloride; sodium; In ammonium hydroxide;
DOI:10.1002/chem.200600815

Reference yield:

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 14344-46-8,403804-61-5
(R)-N-methylcysteine hydrochloride

: 118446-23-4
2-(2-Hydroxyphenyl)-2-thiazoline-4-carboxaldehyde

: Neopyochelin I methyl ester

: Pyochelin II methyl ester

: Neopyochelin II methyl ester

: Pyochelin I methyl ester

Guidance literature:: With potassium acetate; Yield given. Multistep reaction. Yields of byproduct given; 1.) aq. EtOH, 25 deg C, overnight, 2.) ether, MeOH, 0 deg C;
DOI:10.1021/jo00114a029