H-L-PRO-OALL

Base Information

Chemical Name:H-L-PRO-OALL
CAS No.:88224-06-0
Molecular Formula:C8H13 N O2
Molecular Weight:155.197
Hs Code.:2933990090
Mol file:88224-06-0.mol

Synonyms:L-Proline,2-propenyl ester (9CI); Proline, allyl ester (6CI); Allyl(S)-2-pyrrolidinecarboxylate; Allyl L-prolinate

Suppliers and Price of H-L-PRO-OALL

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
H-L-PRO-OALL 95.00%
5MG
$ 495.41

Total 4 raw suppliers

Chemical Property of H-L-PRO-OALL

Chemical Property:

PSA：38.33000
LogP:0.79640

Purity/Quality:

97% ^*data from raw suppliers

H-L-PRO-OALL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of H-L-PRO-OALL

There total 4 articles about H-L-PRO-OALL 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: 81.0%

: 802918-70-3
N-(9-fluorenylmethoxycarbonyl)-proline allyl ester

: 88224-06-0
prop-2-enyl pyrrolidine-2-carboxylate

Guidance literature:: With diethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1021/acs.orglett.6b03056

Reference yield: 72.0%

: 107-18-6
allyl alcohol

: 147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline

: 88224-06-0
prop-2-enyl pyrrolidine-2-carboxylate

Guidance literature:: With silica gel-immobilized perchloric acid; at 80 ℃; for 8h; chemoselective reaction; Inert atmosphere; Neat (no solvent);
DOI:10.1021/jo900614s

Reference yield:

: 71989-31-6
Fmoc-Pro-OH

: 88224-06-0
prop-2-enyl pyrrolidine-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydrogencarbonate / N,N-dimethyl-formamide / 11 h / 20 °C

2: diethylamine / dichloromethane / 2 h / 20 °C

With potassium hydrogencarbonate; diethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acs.orglett.6b03056