Home Cart Sign in  
Chemical Structure| 65360-27-2 Chemical Structure| 65360-27-2
Chemical Structure| 65360-27-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

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-D-Lys(Boc)-OH

CAS No. :65360-27-2
Formula : C16H30N2O6
M.W : 346.42
SMILES Code : O=C(O)[C@H](NC(OC(C)(C)C)=O)CCCCNC(OC(C)(C)C)=O
MDL No. :MFCD00076960
InChI Key :FBVSXKMMQOZUNU-LLVKDONJSA-N
Pubchem ID :7349650

Safety of Boc-D-Lys(Boc)-OH

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

Application In Synthesis of Boc-D-Lys(Boc)-OH

* 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 [ 65360-27-2 ]

[ 65360-27-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7210-76-6 ]
  • [ 65360-27-2 ]
  • C23H38N4O7S [ No CAS ]
YieldReaction ConditionsOperation in experiment
22% Ethyl 2-amino-4-methyl thiazole-5-carboxylate (50 mg, Avocado Research Chemicals LTD), 140 mg of N,N-Di-Boc-lysine, 95 μl of DIEA, and 153 mg of HBTU were dissolved in 1.5 ml of DMF. After stirring at RT for 48 hours, the reaction was quenched by addition of 0.5 ml water and diluted with 40 ml of EtOAc. The organic layer was washed with 1N HCl, brine and worked-up as described in General Procedure. Pure title compound (1B) was obtained by purification on a fresh silica gel column eluted with 30% EtOAc in hexane (30 mg, yield 22%).
 

Historical Records

Categories