Select Region or Location
Americas
  • Argentina
  • Brazil
  • Canada
  • Mexico
  • United States
  • Other Americas
Europe
  • Austria
  • Belgium
  • Bulgaria
  • Croatia/Hrvatska
  • Cyprus
  • Czech Republic
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovak Republic
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • Turkey
  • United Kingdom
  • Other Europe
Asia Pacific
  • Australia
  • China
  • India
  • Indonesia
  • Japan
  • Korea, Republic of
  • Malaysia
  • New Zealand
  • Philippines
  • Singapore
  • Thailand
  • Vietnam
  • Other Asia Pacific
Africa And Middle East
  • Egypt
  • Israel
  • Other Africa And Middle East
USD
Home Cart Sign in  
Chemical Structure| 190332-26-4 Chemical Structure| 190332-26-4

Structure of 190332-26-4

Chemical Structure| 190332-26-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]}{[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}
    {[ size_append_text(item.pr_size, proInfo.prAm, 'list') ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 190332-26-4 ]

CAS No. :190332-26-4
Formula : C10H20O2
M.W : 172.26
SMILES Code : CCCCC(C)CC(C)C(O)=O
English Name :2,4-Dimethyloctanoic acid
MDL No. :MFCD02258576

Safety of [ 190332-26-4 ]

Application In Synthesis of [ 190332-26-4 ]

* 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 [ 190332-26-4 ]

[ 190332-26-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42807-66-9 ]
  • [ 190332-26-4 ]
  • [ 2775434-24-5 ]
YieldReaction ConditionsOperation in experiment
371 mg Stage #1: MeLeu-OBzl p-tosylate With N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole In dichloromethane at 0 - 25℃; Sealed tube; Stage #2: 2,4-dimethyloctanoic acid With benzotriazol-1-ol; copper(ll) bromide In dichloromethane at 20℃; for 24h; Sealed tube; 1.1 Step 1 (Condensation of Racemic 2,4-dimethyloctanoic acid with pTos.N-methyl- L-Leu-OBn). To a round-bottomed, single-necked reaction flask, equipped with a micro magnetic stir bar, is added N,N'-carbonyldiimidazole (CDI) (162 mg), followed by 1 ml of dichloromethane. Gently stirred. The reaction flask is sealed with a rubber septum containing a thermoprobe. The reaction flask is cooled to 0 °C (ice bath). To another round-bottomed, single-necked reaction flask equipped with a micro magnetic stir bar, is added N-Methyl-L-leucine benzyl ester p-toluenesulfonate (pTos.MeN-Leu- OBn) (407 mg), followed by dichloromethane. To the resulting white suspension is added diisopropylethylamine (DIPEA) (129 mg). The suspension turns clear and this is added to the chilled CDI suspension using a syringe over 10 minutes. The suspension turns clear and stirring under a CaCl2 drying tube is continued at room temp (RT) ~25 °C. and is monitored by TLC for completion. The reaction flask is set upon a rotovap and concentrated and extracted twice with ethyl acetate, EtOAc layer is dried over MgSO4, filtered and rotovaped to a viscous oil. [0123] To this oil is added 3 ml of dichloromethane and stirred at RT for 10 minutes and then added 2,4-dimethyloctanoic acid (172 mg), 1-hydroxybenzotriazole hydrate (HOBt hydrate) (2 mg) and CuBr2 (10 mg). The reaction flask is closed with a rubber septum and stirred at RT for 24 h. Upon completion of the reaction (TLC), the mixture is transferred into an Erlenmeyer reaction flask, diluted with dichloromethane and quenched with an aqueous solution of 0.5 N HCl and extracted twice with dichloromethane, washed with NaHCO3, dried over MgSO4, filtered and concentrated by rotovap to give a colourless oil (371 mg) (Intermediate 1.1) LCMS shows correct M+ at 389.570; 95.1 area%.
371 mg Stage #1: MeLeu-OBzl p-tosylate With N-ethyl-N,N-diisopropylamine; 1,1'-carbonyldiimidazole In dichloromethane at 0 - 25℃; Sealed tube; Stage #2: 2,4-dimethyloctanoic acid With benzotriazol-1-ol; copper(ll) bromide In dichloromethane at 20℃; for 24h; Sealed tube; 1.1 Step 1 (Condensation of Racemic 2,4-dimethyloctanoic acid with pTos.N-methyl- L-Leu-OBn). To a round-bottomed, single-necked reaction flask, equipped with a micro magnetic stir bar, is added N,N'-carbonyldiimidazole (CDI) (162 mg), followed by 1 ml of dichloromethane. Gently stirred. The reaction flask is sealed with a rubber septum containing a thermoprobe. The reaction flask is cooled to 0 °C (ice bath). To another round-bottomed, single-necked reaction flask equipped with a micro magnetic stir bar, is added N-Methyl-L-leucine benzyl ester p-toluenesulfonate (pTos.MeN-Leu- OBn) (407 mg), followed by dichloromethane. To the resulting white suspension is added diisopropylethylamine (DIPEA) (129 mg). The suspension turns clear and this is added to the chilled CDI suspension using a syringe over 10 minutes. The suspension turns clear and stirring under a CaCl2 drying tube is continued at room temp (RT) ~25 °C. and is monitored by TLC for completion. The reaction flask is set upon a rotovap and concentrated and extracted twice with ethyl acetate, EtOAc layer is dried over MgSO4, filtered and rotovaped to a viscous oil. [0123] To this oil is added 3 ml of dichloromethane and stirred at RT for 10 minutes and then added 2,4-dimethyloctanoic acid (172 mg), 1-hydroxybenzotriazole hydrate (HOBt hydrate) (2 mg) and CuBr2 (10 mg). The reaction flask is closed with a rubber septum and stirred at RT for 24 h. Upon completion of the reaction (TLC), the mixture is transferred into an Erlenmeyer reaction flask, diluted with dichloromethane and quenched with an aqueous solution of 0.5 N HCl and extracted twice with dichloromethane, washed with NaHCO3, dried over MgSO4, filtered and concentrated by rotovap to give a colourless oil (371 mg) (Intermediate 1.1) LCMS shows correct M+ at 389.570; 95.1 area%.
 

Historical Records

Technical Information

Categories