Home Cart Sign in  
Chemical Structure| 732231-41-3 Chemical Structure| 732231-41-3

Structure of 732231-41-3

Chemical Structure| 732231-41-3

*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 [ 732231-41-3 ]

CAS No. :732231-41-3
Formula : C7H13NO2
M.W : 143.18
SMILES Code : O=C(OC)[C@@H](N)CC1CC1

Safety of [ 732231-41-3 ]

Application In Synthesis of [ 732231-41-3 ]

* 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 [ 732231-41-3 ]

[ 732231-41-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 67-56-1 ]
  • [ 102735-53-5 ]
  • [ 732231-41-3 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; at 0℃; for 16h;Inert atmosphere; Reflux; To a stirred solution of <strong>[102735-53-5](S)-2-amino-3-cyclopropylpropanoic acid</strong> (2 g, 15.50 mmol) in MeOH (20 mL) under an argon atmosphere was added thionyl chloride (3.3 mL, 46.51 mmol) at 0 oC. The reaction mixture was refluxed for 16 h. After consumption of the starting material (monitored by TLC), the volatile components were evaporated in vacuo to obtain methyl (S)-2-amino-3-cyclopropylpropanoate (2.2 g, crude) as a pale yellow solid used in the next step without further purification. LCMS: 144.7 (M+1); (column; Eclipse XDB C-18 (150 × 4.6 mm, 5 mum); RT 1.62 min. 0.05percent Aq TFA; ACN 0.8 mL/min); TLC: 5percent MeOH/ CH2Cl2 (Rf: 0.3).
With thionyl chloride; at 0℃; for 16h;Inert atmosphere; Reflux; Synthesis of methyl (S)-2-amino-3-cyclopropylpropanoate To a stirred solution of <strong>[102735-53-5](S)-2-amino-3-cyclopropylpropanoic acid</strong> (2 g, 15.50 mmol) in MeOH (20 mL) under an argon atmosphere was added thionyl chloride (3.3 mL, 46.51 mmol) at 0° C. The reaction mixture was refluxed for 16 h. After consumption of the starting material (monitored by TLC), the volatile components were evaporated in vacuo to obtain methyl (S)-2-amino-3-cyclopropylpropanoate (2.2 g, crude) as a pale yellow solid used in the next step without further purification. LCMS: 144.7 (M+1); (column; Eclipse XDB C-18 (150*4.6 mm, 5 mum); RT 1.62 min. 0.05percent Aq TFA; ACN 0.8 mL/min); TLC: 5percent MeOH/CH2Cl2 (Rf: 0.3).
 

Historical Records