Home Cart Sign in  
Chemical Structure| 274685-72-2 Chemical Structure| 274685-72-2

Structure of 274685-72-2

Chemical Structure| 274685-72-2

*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 [ 274685-72-2 ]

CAS No. :274685-72-2
Formula : C12H20N2O4
M.W : 256.30
SMILES Code : O=C(C1(NC(N2CCOCC2)=O)CCCCC1)O

Safety of [ 274685-72-2 ]

Application In Synthesis of [ 274685-72-2 ]

* 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 [ 274685-72-2 ]

[ 274685-72-2 ] Synthesis Path-Downstream   1~1

  • 1
  • Morpholine carbonyl chloride [ No CAS ]
  • [ 63203-48-5 ]
  • [ 274685-72-2 ]
YieldReaction ConditionsOperation in experiment
33% Reference Example 5 Synthesis of 1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxylic acid STR9 The same reaction procedure as used in Reference Example 4 was repeated by using 4.36 g (21 mmol) of <strong>[63203-48-5]ethyl 1-aminocyclohexanecarboxylate hydrochloride</strong> and 3.15 g (21 mmol) of morpholine carbonyl chloride, whereby 1.8 g of the captioned 1-[N-(morpholine-4-carbonyl)amino]cyclohexanecarboxylic acid was obtained in a yield of 33%. 1H-NMR (delta, CDCl3): 1.30-1.50 (3H, m), 1.60-1.80 (3H, m), 1.90-2.15 (4H, m), 3.26-3.50 (4H, m), 3.60-3.80 (4H, m), 4.49 (1H, s).
 

Historical Records