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(R)-N-Boc-4-fluorophenylglycine

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(R)-N-Boc-4-fluorophenylglycine Basic information
Product Name:(R)-N-Boc-4-fluorophenylglycine
Synonyms:(D)-N-TERT-BUTOXYCARBONYL-ALPHA-(4-FLUOROPHENYL)ACETIC ACID;BOC-4-FLUORO-D-PHENYLGLYCINE;(R)-N-boc-4-Fluorophenylglycine(e.e.);(R)-N-BOC-4-FLUOROPHENYLGLYCINE 95% (98% E.E.);(R)-N-Boc-4-fluorophenylglycine, 95%, ee:98%;(R)-N-BOC-4-Fluorophenylglycine, 98% ee;(R)-N-BOC-4-Fluorophenylglycine, 98% ee, 95% 1GR;Boc-(R)-2-amino-2-(4-fluorophenyl)acetic acid
CAS:196707-32-1
MF:C13H16FNO4
MW:269.27
EINECS:
Product Categories:
Mol File:196707-32-1.mol
(R)-N-Boc-4-fluorophenylglycine Structure
(R)-N-Boc-4-fluorophenylglycine Chemical Properties
Melting point 85.7 °C
Boiling point 408.4±40.0 °C(Predicted)
density 1.2168 (estimate)
storage temp. Sealed in dry,Room Temperature
form Powder
pka3.47±0.10(Predicted)
color White
CAS DataBase Reference196707-32-1
Safety Information
Safety Statements 24/25
HazardClass IRRITANT
HS Code 29224985
MSDS Information
ProviderLanguage
ACROS English
(R)-N-Boc-4-fluorophenylglycine Usage And Synthesis
Chemical Propertieswhite powder
Synthesis
Di-tert-butyl dicarbonate

24424-99-5

(4-FLUORO-PHENYLAMINO)-ACETIC ACID

351-95-1

(R)-N-BOC-4-FLUOROPHENYLGLYCINE

196707-32-1

Example 59a Single Enantiomeric Isomer; R Configuration NaHCO3 (1.0 g, 11.9 mmol) was added to a stirred aqueous suspension of (R)-4-fluorophenylglycine (1.0 g, 5.9 mmol). after 30 min, a solution of di-tert-butyl dicarbonate (1.5 g, 7.1 mmol) dissolved in tertiary butanol was slowly added dropwise. The reaction mixture was stirred overnight at room temperature. Upon completion of the reaction, the reaction mixture was diluted with water and the pH was subsequently adjusted to 4-5 with 5% aqueous citric acid.The mixture was extracted with dichloromethane (DCM), the organic layer was separated, dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the title compound (R)-2-((tert-butoxycarbonyl)amino)-2-(4-fluorophenyl)acetic acid (1.6 g). HPLC-MS (Method 17): retention time (Rt) = 2.25 min; mass spectrum (ES+): m/z = 292 [M + Na]+.

References[1] Patent: US2015/105397, 2015, A1. Location in patent: Paragraph 0385; 0386; 0387; 0388; 0389
(R)-N-Boc-4-fluorophenylglycine Preparation Products And Raw materials
Raw materialsDi-tert-butyl dicarbonate-->(4-Fluoro-phenylamino)-acetic acid-->(R)-4-Fluorophenylglycine-->tert-Butanol-->Sodium bicarbonate
Tag:(R)-N-Boc-4-fluorophenylglycine(196707-32-1) Related Product Information
(S)-N-Boc-4-fluorophenylglycine (S)-1-(4-Fluorophenyl)ethylamine tert-Butoxycarbonylamino-phenyl-acetic acid Boc-D-Phg-OH (R)-N-(tert-Butoxycarbonyl)-2-phenylglycinol 4-Fluorophenylglycine (R)-4-Fluorophenylglycine 4-Fluorophenylacetic acid N-Boc-d/L-phenylglycinol For-D-Phg-OH (S)-N-Methyl-1-(4-fluorophenyl)ethylamine (R)-N-Boc-4-fluorophenylglycine (S) (-)-alpha-Phenethylurethane 4-Fluorophenylglycine-N-Boc protected N-Me-D-Phg-OH 2-Fluorophenylglycine-N-Boc protected (R)-tert-Butoxycarbonylamino-(2,4-difluoro-phenyl)-acetic acid (R)-tert-Butoxycarbonylamino-(3,4-difluoro-phenyl)-acetic acid