Home Cart Sign in  
Chemical Structure| 233691-67-3 Chemical Structure| 233691-67-3
Chemical Structure| 233691-67-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Boc-Lys(Ac)-Amc-OH is a cell-permeable fluorescent HDAC substrate with excitation/emission wavelengths of 355 nm/460 nm.

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-Lys(Ac)-Amc-OH

CAS No. :233691-67-3
Formula : C23H31N3O6
M.W : 445.51
SMILES Code : O=C(OC(C)(C)C)N[C@@H](CCCCNC(C)=O)C(NC1=CC(O2)=C(C=C1)C(C)=CC2=O)=O
MDL No. :MFCD02683946
InChI Key :SUTRDULVNIPNLW-SFHVURJKSA-N
Pubchem ID :9846360

Safety of Boc-Lys(Ac)-Amc-OH

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

Application In Synthesis of Boc-Lys(Ac)-Amc-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 [ 233691-67-3 ]

[ 233691-67-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 26093-31-2 ]
  • [ 6404-26-8 ]
  • [ 233691-67-3 ]
YieldReaction ConditionsOperation in experiment
65% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 0 - 60℃; for 24h; Dipeptide 47 was synthesized by following the above general procedure for HATU peptide coupling (0 - 60C) for 12 hours and purified by silica gel column (0226) chromatography (EtOAc: Hexane - 3: 1) as a white solid (yield: 65%). lH NMR (400 MHz, CDC13) delta ppm: 9.34 (bs, 1 H), 7.69 (s, 1 H), 7.55 - 7.36 (m, 2 H), 6.79 (bs, 1 H), 5.55 (d, J = 7.2 Hz, 1 H), 4.41 - 4.16 (m, 1 H), 3.35 - 3.26 (m, 2 H), 2.39 (s, 3 H), 2.07 (s, 3 H), 2.00 - 1.87 (m, 1 H), 1.74 (dd, J = 4.9, 13.5 Hz, 1 H), 1.65 - 1.54 (m, 3 H), 1.53 - 1.47 (m, 1 H), 1.45 (s, 9 H), 1.30 - 1.20 (m, 1 H), 1.20 - 1.11 (m, 1 H). MS (ESI): found: [M + Na]+, 468.4.
With triethylamine; HATU; In N,N-dimethyl-formamide; at 20℃; for 2h; To a solution of 8w in DMF at room temperature was added 7-amino-4-methyl- 2H-chromen-2-one, HATU and triethylamine. The reaction was stirred at room temperature for 2 h. A saturated solution of sodium bicarbonate was added. The product was extracted with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by prep-HPLC to afford 9w.
With HATU; triethylamine; In N,N-dimethyl-formamide; at 20℃; for 2h; To a solution of 8w in DMF at room temperature was added 7-amino-4-methyl-2H-chromen-2-one, HATU and triethy247lamine. The reaction was stirred at room temperature for 2 h. A saturated solution of sodium bicarbonate was added. The product was extracted with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by prep-HPLC to afford 9w
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20℃; for 2h; To a solution of 8w in DMF at room temperature was added 7-amino-4-methyl-2H-chromen-2-one, HATU and triethylamine. The reaction was stirred at room temperature for 2 h. A saturated solution of sodium bicarbonate was added. The product was extracted with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude residue was purified by prep-HPLC to afford 9w.

 

Historical Records

Categories