Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Glycine derivative >  N-BOC-D-CYCLOHEXYLGLYCINOL

N-BOC-D-CYCLOHEXYLGLYCINOL

Basic information Safety Supplier Related

N-BOC-D-CYCLOHEXYLGLYCINOL Basic information

Product Name:
N-BOC-D-CYCLOHEXYLGLYCINOL
Synonyms:
  • BOC-D-CYCLOHEXYLGLYCINOL
  • BOC-D-CHG-OL
  • N-BOC-D-CYCLOHEXYLGLYCINOL
  • N-T-BOC-D-CYCLOHEXYLGLYCINOL
  • N-T-BUTOXYCARBONYL-D-CYCLOHEXYLGLYCINOL
  • tert-butyl N-[(1R)-1-cyclohexyl-2-hydroxyethyl]carbamate
  • -tert-Butyl (1-cyclohexyl-2-hydroxyethyl)
  • N-Boc-D-2-amino-2-cyclohexylethanol,99%e.e.
CAS:
188348-00-7
MF:
C13H25NO3
MW:
243.34
Product Categories:
  • Amino Acid Derivatives
  • Amino Alcohols
  • Peptide Synthesis
Mol File:
188348-00-7.mol
More
Less

N-BOC-D-CYCLOHEXYLGLYCINOL Chemical Properties

Melting point:
83-87 °C(lit.)
Boiling point:
371.2±25.0 °C(Predicted)
Density 
1.037±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
pka
12.07±0.46(Predicted)
form 
solid
Appearance
White to off-white Solid
optical activity
[α]20/D +13°, c = 1% in chloroform
CAS DataBase Reference
188348-00-7
More
Less

Safety Information

Hazard Codes 
Xn,N
Risk Statements 
22-36/37/38-50/53
Safety Statements 
26-60-61
RIDADR 
UN 3077 9/PG 3
WGK Germany 
3
HS Code 
2906190090

MSDS

More
Less

N-BOC-D-CYCLOHEXYLGLYCINOL Usage And Synthesis

Uses

peptide synthesis

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

70491-05-3

188348-00-7

General procedure for the synthesis of tert-butyl (R)-(1-cyclohexyl-2-hydroxyethyl)carbamate from (R)-2-((tert-butoxycarbonyl)amino)-2-cyclohexylacetic acid: N-(tert-butoxycarbonyl)cyclohexylglycine (2.0 g, 7.77 mmol) was dissolved in anhydrous THF (10 mL) and the solution was cooled to 0 °C. Borane-THF solution (1 M solution of THF, 15.5 mL, 15.5 mmol) was added slowly under stirring. After addition, the reaction mixture was gradually warmed to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the reaction was carefully quenched with methanol (5 mL), followed by evaporation of the volatiles under reduced pressure. The organic layer was separated by partitioning the residue between water and ethyl acetate. The organic layer was washed sequentially with saturated aqueous sodium bicarbonate, brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford the target product tert-butyl-(1-cyclohexyl-2-hydroxyethyl)carbamate (1.26 g, 66.7% yield). Mass spectrum (chemical ionization) m/z 144.20 (MH+-BOC).

References

[1] Journal of Medicinal Chemistry, 2004, vol. 47, # 14, p. 3483 - 3486
[2] Patent: WO2005/7164, 2005, A1. Location in patent: Page 28-29
[3] Patent: WO2005/7165, 2005, A1. Location in patent: Page 36
[4] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 4, p. 865 - 868

N-BOC-D-CYCLOHEXYLGLYCINOLSupplier

Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Daicel Chiral Technologies (China)CO.,LTD
Tel
021-50460086-9 15921403865
Email
han_yajun@dctc.daicel.com
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Email
mlcheng@sunwaypharm.cn