Home Cart Sign in  
Chemical Structure| 138775-03-8 Chemical Structure| 138775-03-8

Structure of 138775-03-8

Chemical Structure| 138775-03-8

*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 [ 138775-03-8 ]

CAS No. :138775-03-8
Formula : C18H24N2O6
M.W : 364.39
SMILES Code : O=C(N1[C@H](C(O)=O)CN(C(OCC2=CC=CC=C2)=O)CC1)OC(C)(C)C
MDL No. :MFCD02179111
InChI Key :SREPAMKILVVDSP-AWEZNQCLSA-N
Pubchem ID :7010652

Safety of [ 138775-03-8 ]

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

Application In Synthesis of [ 138775-03-8 ]

* 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 [ 138775-03-8 ]

[ 138775-03-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 23357-46-2 ]
  • [ 138775-03-8 ]
  • [ 913359-59-8 ]
YieldReaction ConditionsOperation in experiment
Step 1 :(S)-4-(Benzyloxycarbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1.00 g, 2.70 mmol), HOBt (520 mg, 3.80 mmol), HBTU (1.35 g, 3.60 mmol) and DIPEA (955 uL, 5.50 mmol) were dissolved in dry DMF (10 ml) under N2 and stirred for 10 minutes at room temperature. R-1,2,3,4-Tetrahydro-1-naphtylamine (485 mg, 3.30 mmol) was added and <n="83"/>the solution was left to stir for 18 hours at room temperature. The contents were then added to a separatory funnel along with EtOAc and washed with 10% citric acid, saturated NaHCO3 and brine. The organic layer was collected, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to provide intermediate 5-a as a white solid.
 

Historical Records

Technical Information

Categories