Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Glycine derivative >  (R)-N-BOC-4-FLUOROPHENYLGLYCINE

(R)-N-BOC-4-FLUOROPHENYLGLYCINE

Basic information Safety Supplier Related

(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
Mol File:
196707-32-1.mol
More
Less

(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
pka
3.47±0.10(Predicted)
color 
White
CAS DataBase Reference
196707-32-1
More
Less

Safety Information

Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
29224985

MSDS

  • Language:English Provider:ACROS
More
Less

(R)-N-BOC-4-FLUOROPHENYLGLYCINE Usage And Synthesis

Chemical Properties

white powder

Synthesis

24424-99-5

351-95-1

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-FLUOROPHENYLGLYCINESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Email
sales@maya-r.com
Thermo Fisher Scientific
Tel
800-810-5118
Email
cnchemical@thermofisher.com