N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Base Information

Chemical Name:N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide
CAS No.:106086-14-0
Molecular Formula:C15H20 N2 O3 S
Molecular Weight:308.3959
Hs Code.:
DSSTox Substance ID:DTXSID70909899

Synonyms:BRN 5591302;106086-14-0;N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide;3-Thiazolidinecarboxylic acid, 4-(aminocarbonyl)-2-phenyl-, 1,1-dimethylethyl ester;4-(Aminocarbonyl)-2-phenyl-3-thiazolidinecarboxylic acid 1,1-dimethylethyl ester;DTXSID70909899;LS-151167;3-(tert-Butoxycarbonyl)-2-phenyl-1,3-thiazolidine-4-carboximidic acid

Suppliers and Price of N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Chemical Property:

Vapor Pressure:1.44E-10mmHg at 25°C
Boiling Point:511.3°C at 760 mmHg
Flash Point:263°C
Density:1.238g/cm³
XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:308.11946368
Heavy Atom Count:21
Complexity:402

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1C(CSC1C2=CC=CC=C2)C(=O)N

Technology Process of N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

There total 4 articles about N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide 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: 85.0%

: 106086-12-8
N-Oxysuccinimide N'-tert-butyloxycarbonyl-2-phenylthiazolidine-4-carboxylate

: 106086-14-0
N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Guidance literature:: With ammonia; In methanol; for 1.5h; Ambient temperature;
DOI:10.1007/BF01148643

Reference yield:

: 196930-46-8
(4R)-2-phenyl-1,3-thiazolidine-4-carboxylic acid

: 106086-14-0
N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / Et₃N / dimethylformamide / 2 h / Ambient temperature

2: 81 percent / pyridine / dimethylformamide / 2 h / Ambient temperature

3: 85 percent / NH₃ / methanol / 1.5 h / Ambient temperature

With pyridine; ammonia; triethylamine; In methanol; N,N-dimethyl-formamide;
DOI:10.1007/BF01148643

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 106086-14-0
N-tert-Butyloxycarbonyl-2-phenylthiazolidine-4-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / Et₃N / dimethylformamide / 2 h / Ambient temperature

2: 81 percent / pyridine / dimethylformamide / 2 h / Ambient temperature

3: 85 percent / NH₃ / methanol / 1.5 h / Ambient temperature

With pyridine; ammonia; triethylamine; In methanol; N,N-dimethyl-formamide;
DOI:10.1007/BF01148643