Home Cart Sign in  
Chemical Structure| 24277-39-2 Chemical Structure| 24277-39-2
Chemical Structure| 24277-39-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Boc-Glu-OtBu is a glutamic acid derivative, commonly used in peptide synthesis and drug development.

Synonyms: Boc-Glu-OtBu

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Boc-Glu-OtBu

CAS No. :24277-39-2
Formula : C14H25NO6
M.W : 303.35
SMILES Code : O=C(O)CC[C@H](NC(OC(C)(C)C)=O)C(OC(C)(C)C)=O
Synonyms :
Boc-Glu-OtBu
MDL No. :MFCD00038273

Safety of Boc-Glu-OtBu

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of Boc-Glu-OtBu

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 24277-39-2 ]

[ 24277-39-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 5672-83-3 ]
  • [ 24277-39-2 ]
  • [ 157886-31-2 ]
  • [ 73872-73-8 ]
  • [ 63061-86-9 ]
  • 2
  • [ 24277-39-2 ]
  • [ 24835-08-3 ]
  • N-(tert-Butoxycarbonyl)-N'-(2-nitrobenzyl)-L-glutamine α-tert-butyl ester [ No CAS ]
  • 4
  • [ 24277-39-2 ]
  • [ 91229-86-6 ]
  • 5
  • [ 7724-12-1 ]
  • [ 24277-39-2 ]
  • tert-butyl N2-(tert-butoxycarbonyl)-N5-(2-cyanobenzo[d]thiazol-6-yl)glutaminate [ No CAS ]
YieldReaction ConditionsOperation in experiment
60% solution of Boc-Glu-OtBu ( 303 mg, 1.0 mmol) was added N-methylmorpholine (82 muL, 1.0 mmol) and i-BuOCOCl (112 muL, 2.0 mmol) in tetrahydrofuran (2 mL), the mixture was stirred at 0 °C for 0.5 h. Then <strong>[7724-12-1]2-cyano-6-aminobenzothiazole</strong> (87 mg, 0.5mmol) in 2ml tetrahydrofuan was added. The mixture was stirred at room temperature overnight. Then the solution was evaporated under reduced pressure. The mixture was diluted with ethyl acetate and (50 mL) washed with saturated sodium bicarbonate solution, water and brine, dried over anhydrous MgSO4 and filtered. The crude product was purified by chromatography with ethyl acetate?hexane (1:2) as the eluents to afford a white solid, 83 mg, yield = 60percent. 1H-NMR (400 MHz, CDCl3) delta 9.87 (s, 1H), 8.79 (s, 1H), 8.12 (d, J = 8.9 Hz, 1H), 7.57 (d, J = 8.8 Hz, 1H), 5.48 (d, J = 7.8 Hz, 1H), 4.30 ? 4.17 (m, 1H), 2.58 ? 2.45 (m, 2H), 2.30 (m, J = 10.3, 7.1, 3.3 Hz, 1H), 1.85 (m, J = 16.2, 10.7, 4.7 Hz, 1H), 1.51 (s, 9H), 1.46 (s, 9H).
 

Historical Records

Categories