Home Cart Sign in  
Chemical Structure| 167834-23-3 Chemical Structure| 167834-23-3

Structure of 167834-23-3

Chemical Structure| 167834-23-3

*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 [ 167834-23-3 ]

CAS No. :167834-23-3
Formula : C16H23NO4
M.W : 293.36
SMILES Code : O=C(OCC)C[C@@H](NC(OC(C)(C)C)=O)C1=CC=CC=C1
MDL No. :MFCD29076768

Safety of [ 167834-23-3 ]

Application In Synthesis of [ 167834-23-3 ]

* 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 [ 167834-23-3 ]

[ 167834-23-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 167834-23-3 ]
  • [ 135865-78-0 ]
YieldReaction ConditionsOperation in experiment
To a dry, cooled (-78° C.) solution of ethyl (3S)-3-[(tert-butoxycarbonyl)amino]-3-phenylpropanoate from Step A (1.00 g, 3.41 mmol) was added a solution of DiBAl-H (6.82 mL, 6.82 mmol, 1 M in CH2Cl2) slowly over 30 min. After an additional 30 min of stirring at -78° C., the reaction was quenched by the rapid addition of saturated aqueous Rochelle's salt (32 mL). The cooling bath was then removed and the reaction was allowed to rapidly stir until a noticeable decrease in the amount of emulsion was observed. The layers were separated and the aqueous layer was extracted with CH2Cl2 (2.x.30 mL). Combined organics were dried over sodium sulfate, filtered and concentrated in vacuo to give an oil. This oil was purified by silica gel chromatography, eluting with a gradient of EtOAc:hexanes 5:95 to 40:60, to give the title compound. MS: m/z=150 (M-CO2C4H7).
With diisobutylaluminium hydride; Synthesis of compounds 69-71 see tableScheme V (for compounds 69-71 )
 

Historical Records