1-(2-Methylacryloyl)-L-proline

Base Information

Chemical Name:1-(2-Methylacryloyl)-L-proline
CAS No.:51161-88-7
Molecular Formula:C9H13NO3
Molecular Weight:183.207
Hs Code.:
DSSTox Substance ID:DTXSID60527884
Nikkaji Number:J351.265G
Wikidata:Q82397105
Mol file:51161-88-7.mol

Synonyms:51161-88-7;N-methacryloyl-L-proline;1-(2-Methylacryloyl)-L-proline;(2S)-1-(2-methylprop-2-enoyl)pyrrolidine-2-carboxylic acid;Methacryloyl-L-proline;MFCD15833019;methacryl-l-proline;starbld0046569;SCHEMBL5013232;DTXSID60527884;SJAYUJDJZUWFDO-ZETCQYMHSA-N;1-(2-methyl-2-propenoyl)-L-proline;AKOS030240671;BS-42881;CS-0137464;D79446;(2S)-1-(2- methyl-2-propenoyl)-2-pyrrolidine carboxylic acid

Suppliers and Price of 1-(2-Methylacryloyl)-L-proline

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
N-Methacryloyl-L-proline
250mg
$ 150.00

TRC
N-Methacryloyl-L-proline
2.5g
$ 1190.00

Medical Isotopes, Inc.
N-Methacryloyl-L-proline
250 mg
$ 650.00

Total 5 raw suppliers

Chemical Property of 1-(2-Methylacryloyl)-L-proline

Chemical Property:

Melting Point:98-100oC
PSA：57.61000
LogP:0.57600
Storage Temp.:Refrigerator
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:183.08954328
Heavy Atom Count:13
Complexity:260

Purity/Quality:

99% ^*data from raw suppliers

N-Methacryloyl-L-proline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=C)C(=O)N1CCCC1C(=O)O
Isomeric SMILES:CC(=C)C(=O)N1CCC[C@H]1C(=O)O
Uses N-Methacryloyl-L-proline is a reactant used in the preparation of affinity ligands for the androstane receptor.

Technology Process of 1-(2-Methylacryloyl)-L-proline

There total 5 articles about 1-(2-Methylacryloyl)-L-proline 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: 91.0%