Home Cart Sign in  
Chemical Structure| 38854-94-3 Chemical Structure| 38854-94-3

Structure of 38854-94-3

Chemical Structure| 38854-94-3

*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 [ 38854-94-3 ]

CAS No. :38854-94-3
Formula : C12H13NO3
M.W : 219.24
SMILES Code : O=C([C@@H](CC1)N(CC2=CC=CC=C2)C1=O)O
MDL No. :MFCD00797914

Safety of [ 38854-94-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 38854-94-3 ]

* 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 [ 38854-94-3 ]

[ 38854-94-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38854-94-3 ]
  • [ 4089-07-0 ]
  • N-(benzyl)-L-pyroglutamyl-L-tyrosine ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In ethyl acetate; N,N-dimethyl-formamide; Example 37 Synthesis of N-(Benzyl)-L-pyroglutamyl-L-tyrosine Ethyl Ester To a solution of N-benzyl-L-pyroglutamic acid (J. Am. Chem. Soc. 106:4539 (1984), 1.00 g, 4.56 mmol), <strong>[4089-07-0]L-<strong>[4089-07-0]tyrosine ethyl ester hydrochloride</strong></strong> (1.23 g, 5.01 mmol) and BOP (2.22 g, 5.01 mmol) in DMF (32 mL) under nitrogen was added triethylamine (1.14 g, 11.26 mmol) dropwise and the resulting solution was stirred at ambient temperature for 22.5 h. The reaction was quenched by addition of 150 mL of saturated sodium bicarbonate and 150 mL of EtOAc. The organic layer was separated and washed sequentially with 150 mL H2O, 150 mL 10percent citric acid and 150 mL saturated brine, dried over MgSO4 and evaporated to 1.6 g (82percent) of a white solid, mp 192-194° C. Physical data was as follows: 1H NMR (DMSO-d6, 400 MHz) delta 9.23 (s, 1H); 8.52 (d, 1H, J=7.9 Hz); 7.32-7.23 (m, 3H); 7.03-6.97 (m, 4H); 6.69-6.65 (m, 2H); 4.75 (d, 1H, J=15.2 Hz); 4.49-4.43 (m, 1H); 4.11-4.01 (m, 2H); 3.88-3.85 (m, 1H); 3.37 (d, 1H, J=15.2 Hz); 2.99-2.94 (m, 1H); 2.78-2.72 (m, 1H); 2.33-2.08 (m, 3H); 1.98 (s, 0.2H); 1.76-1.70 (m, 1H); 1.14 (t, 3H, J=7.25 Hz). IR (KBr, cm-1) 3400; 3250; 3060; 1725; 1680; 1670; 1550; 1510; 1440; 1265; 1220. MS (-FAB) 409.1 (M-H); 381.0; 302.0; 275.0; 257.0; 217.0; 183.0; 91.0. Anal. Calc'd for C23H26N2O5.0.2M EtOAc: C, 66.78; H, 6.50; N, 6.54. Found: C, 66.48; H, 6.35; N, 6.66.
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In ethyl acetate; N,N-dimethyl-formamide; Example 37 Synthesis of N-(Benzyl)-L-pyroglutamyl-L-tyrosine Ethyl Ester To a solution of N-benzyl-L-pyroglutamic acid (J.Am. Chem. Soc. 106:4539 (1984), 1.00 g, 4.56 mmol), <strong>[4089-07-0]L-<strong>[4089-07-0]tyrosine ethyl ester hydrochloride</strong></strong> (1.23 g, 5.01 mmol) and BOP (2.22 g, 5.01 mmol) in DMF (32 mL) under nitrogen was added triethylamine (1.14 g, 11.26 mmol) dropwise and the resulting solution was stirred at ambient temperature for 22.5 h. The reaction was quenched by addition of 150 mL of saturated sodium bicarbonate and 150 mL of EtOAc. The organic layer was separated and washed sequentially with 150 mL H2O, 150 mL 10percent citric acid and 150 mL saturated brine, dried over MgSO4 and evaporated to 1.6 g (82percent) of a white solid, mp 192-194°C. Physical data was as follows: 1H NMR (DMSO-d6, 400 MHz) delta 9.23 (s, 1H); 8.52 (d, 1H, J = 7.9 Hz); 7.32-7.23 (m, 3H); 7.03-6.97 (m, 4H); 6.69-6.65 (m, 2H); 4.75 (d, 1H, J = 15.2 Hz); 4.49-4.43 (m, 1H); 4.11-4.01 (m, 2H); 3.88-3.85 (m, 1H); 3.37 (d, 1H, J=15.2 Hz); 2.99-2.94 (m, 1H); 2.78-2.72 (m, 1H); 2.33-2.08 (m, 3H); 1.98 (s, 0.2H); 1.76-1.70 (m, 1H); 1.14 (t, 3H, J=7.25 Hz). IR (KBr, cm-1) 3400; 3250; 3060; 1725; 1680; 1670; 1550; 1510; 1440; 1265; 1220. MS (-FAB) 409.1 (M - H); 381.0; 302.0; 275.0; 257.0; 217.0; 183.0; 91.0. Anal. Calc'd for C23H26N2O5 * 0.2M EtOAc: C, 66.78; H, 6.50; N, 6.54. Found: C, 66.48; H, 6.35; N, 6.66.
 

Historical Records