Home Cart Sign in  
Chemical Structure| 37535-58-3 Chemical Structure| 37535-58-3
Chemical Structure| 37535-58-3

*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-4-Pal-OH

CAS No. :37535-58-3
Formula : C13H18N2O4
M.W : 266.29
SMILES Code : O=C(O)[C@H](NC(OC(C)(C)C)=O)CC1=CC=NC=C1
MDL No. :MFCD00672529

Safety of Boc-D-4-Pal-OH

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

Application In Synthesis of Boc-D-4-Pal-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 [ 37535-58-3 ]

[ 37535-58-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6972-82-3 ]
  • [ 37535-58-3 ]
  • (R)-tert-butyl 1-(6-amino-1-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-ylamino)-1-oxo-3-(pyridin-4-yl)propan-2-ylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N,N-dimethyl-formamide; In N,N-dimethyl-formamide; at 26℃; for 18h;Inert atmosphere; To a mixture of (R)-2-(tert-butoxycarbonyl amino)-3 -(pyridin-4-yl)propanoic acid (2.0 mmol, 0.533 g) and 5,6-diamino- 1 -methylpyrimidine-2,4(1H,3H)-dione (2.0 mmol, 0.3 12 g) in DMF (15 mL) was added DCC (8.0 mmol, 1.70 g). The reaction mixture was stirred at 26 °C for 1 8h under N2 atmosphere. The reaction was concentrated and purified by flash chromatography (MeOHIEA=1/3) to give the product; ESI: m/z 405.2 (M+H).
 

Historical Records