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Boc-L-3-benzothienylalanine

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Boc-L-3-benzothienylalanine Basic information
Product Name:Boc-L-3-benzothienylalanine
Synonyms:RARECHEM BK PT 0204;N-ALPHA-T-BOC-BETA-(3-BENZOTHIENYL)-L-ALANINE;N-ALPHA-T-BUTOXYCARBONYL-3-(3-BENZOTHIENYL)-L-ALANINE;BOC-3-(3-BENZOTHIENYL)-L-ALANINE;BOC-L-3-BENZOTHIENYLALA;BOC-L-3-(3-BENZOTHIENYL)ALANINE;BOC-BTA-OH;BOC-ALA(3-BENZOTHIENYL)-OH
CAS:154902-51-9
MF:C16H19NO4S
MW:321.39
EINECS:
Product Categories:Phenylalanine analogs and other aromatic alpha amino acids;Amino Acids;Amino Acid Derivatives;a-amino
Mol File:154902-51-9.mol
Boc-L-3-benzothienylalanine Structure
Boc-L-3-benzothienylalanine Chemical Properties
Boiling point 514.1±45.0 °C(Predicted)
density 1.274±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
pka3.85±0.10(Predicted)
AppearanceWhite to off-white Solid
BRN 7081201
Major Applicationpeptide synthesis
InChI1S/C16H19NO4S/c1-16(2,3)21-15(20)17-12(14(18)19)8-10-9-22-13-7-5-4-6-11(10)13/h4-7,9,12H,8H2,1-3H3,(H,17,20)(H,18,19)/t12-/m0/s1
InChIKeyMURVSBJYXHTRJQ-LBPRGKRZSA-N
SMILESCC(C)(C)OC(=O)N[C@@H](Cc1csc2ccccc12)C(O)=O
CAS DataBase Reference154902-51-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
WGK Germany 3
10-23
HazardClass IRRITANT
HS Code 2934999090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Boc-L-3-benzothienylalanine Usage And Synthesis
Usespeptide synthesis
reaction suitabilityreaction type: Boc solid-phase peptide synthesis
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

L-3-BENZOTHIENYLALANINE

72120-71-9

BOC-L-3-BENZOTHIENYLALANINE

154902-51-9

General procedure for the synthesis of (S)-3-(benzo[b]thiophen-3-yl)-2-((tert-butoxycarbonyl)amino)propionic acid from di-tert-butyl dicarbonate and (S)-2-amino-3-(benz[b]thiophen-3-yl)propionic acid: to a THF:H2O (1.0 g, 4.52 mmol) solution containing K2CO3 (0.75 g, 5.33 mmol) and (S)-2-amino-3-(benzo[b]thieno -3-yl)propionic acid (1.0 g, 4.52 mmol) to a solution of THF:H2O (1:1, v/v) was slowly added di-tert-butyl dicarbonate (1.09 g, 5 mmol). Subsequently, the reaction mixture was gradually warmed to room temperature and stirred continuously overnight. Upon completion of the reaction, the mixture was concentrated to remove most of the solvent and then the residue was dissolved in a mixture of EtOAc and H2O. The pH of the aqueous phase was adjusted to 1-2 with 6N HCl, followed by three extractions with EtOAc. The organic layers were combined, dried with anhydrous Na2SO4, filtered and concentrated to give 1.22 g of the target product as a white foamy solid in 84% yield.

References[1] Journal of Medicinal Chemistry, 1994, vol. 37, # 13, p. 2090 - 2099
[2] Patent: WO2005/85227, 2005, A1. Location in patent: Page/Page column 47; 117
Boc-L-3-benzothienylalanine Preparation Products And Raw materials
Raw materialsDi-tert-butyl dicarbonate-->L-3-Benzothienylalanine-->Potassium carbonate-->Water-->Tetrahydrofuran
Tag:Boc-L-3-benzothienylalanine(154902-51-9) Related Product Information
Boc-L-2-aminomethylphe(Fmoc) Boc-(S)-alpha-(3-benzothiophenylmethyl)-proline Boc-3-(3-benzothienyl)-DL-alanine Boc-D-3-benzothienylalanine Boc-L-3-thienylalanine dcha salt Boc-DL-3-thienylalanine (2-Thiophen-3-yl-ethyl)-carbamic acid tert-butyl ester Boc-L-3-benzothienylalanine L-3-Benzothienylalanine 3-Thiophenepropionic acid 3-Thien-3-ylpropanoic acid L-3-Thienylalanine Thianaphthene 3-(3-benzo(b)thienyl)alanine 3-(Benzo[b]thiophen-3-yl)propanoicacid