O-Methylserine

Base Information

Chemical Name:O-Methylserine
CAS No.:4219-94-7
Molecular Formula:C₄H₉NO₃
Molecular Weight:119.12
Hs Code.:
European Community (EC) Number:859-976-9
UNII:R5MJK98YKK
DSSTox Substance ID:DTXSID60941607
Nikkaji Number:J253.922E
Wikidata:Q27144909
Metabolomics Workbench ID:87127
ChEMBL ID:CHEMBL4085261
Mol file:4219-94-7.mol

Synonyms:O-methylserine;O-methylserine, (D)-isomer;O-methylserine, (DL)-isomer;O-methylserine, (L)-isomer

Suppliers and Price of O-Methylserine

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

American Custom Chemicals Corporation
O-METHYLSERINE 95.00%
1G
$ 850.00

American Custom Chemicals Corporation
O-METHYLSERINE 95.00%
250MG
$ 654.00

Total 15 raw suppliers

Chemical Property of O-Methylserine

Chemical Property:

Vapor Pressure:0.00363mmHg at 25°C
Boiling Point:260.6°Cat760mmHg
Flash Point:111.4°C
PSA：72.55000
Density:1.195g/cm³
LogP:-0.25500
Water Solubility.:soluble
XLogP3:-3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:119.058243149
Heavy Atom Count:8
Complexity:83.4

Purity/Quality:

97% ^*data from raw suppliers

O-METHYLSERINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: S24/25:;

MSDS Files:

Useful:

Canonical SMILES:COCC(C(=O)O)N
Isomeric SMILES:COC[C@@H](C(=O)O)N

Technology Process of O-Methylserine

There total 11 articles about O-Methylserine 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: 99.9%

: 98026-05-2
α-amino-β-methoxy-propionamide

: 4219-94-7,19794-53-7,32620-11-4,86118-11-8
DL-3-methoxy-alanine

Guidance literature:: With α-amino-ε-caprolactam racemase; peptidase B; at 38 ℃; for 18h; Enzymatic reaction;
DOI:10.1016/j.tetasy.2012.11.006

Reference yield: 50.0%

: 98632-99-6
O-Methyl-N-acetyl-DL-serine

: 4219-94-7,19794-53-7,32620-11-4,86118-11-8
DL-3-methoxy-alanine

: 196601-67-9
(R)-2-N-acetamido-3-methoxypropionic acid

Guidance literature:: With sodium hydroxide; acylase I from porcine kidney; In water; at 25 ℃; pH=7.5 - 8; Product distribution / selectivity; Enzymatic reaction; Resolution of racemate;