Home Cart Sign in  
Chemical Structure| 3619-74-7 Chemical Structure| 3619-74-7

Structure of 3619-74-7

Chemical Structure| 3619-74-7

*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 [ 3619-74-7 ]

CAS No. :3619-74-7
Formula : C8H18N2
M.W : 142.24
SMILES Code : CCCN1CCNCCC1
MDL No. :MFCD09055331

Safety of [ 3619-74-7 ]

Application In Synthesis of [ 3619-74-7 ]

* 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 [ 3619-74-7 ]

[ 3619-74-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 497-19-8 ]
  • [ 599-91-7 ]
  • [ 3619-74-7 ]
YieldReaction ConditionsOperation in experiment
In ethanol; water; EXAMPLE 23 8-chloro-10,11-dihydro-10-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)carbonyl]dibenz[b,f][1,4]oxazepine STR30 A mixture of the product of Example 96 (37.0 g, 0.21 mole), n-<strong>[599-91-7]propyl tosylate</strong> (68.1 g, 0.31 mole), Na2 CO3 (16.8 g, 0.16 mole), and 160 mL of EtOH were refluxed for 14 hours under N2. After cooling the reaction, it was filtered and all solvent was removed from the filtrate under reduced pressure. The residue was mixed with 300 mL of water and extracted with 2*200 mL of Et2 O. The product HCl salt was precipitated and converted to hexahydro-1-propyl-1H-1,4-diazacycloheptane by the methods of Example 21.
In ethanol; water; Example 23 8-chloro-10,11-dihydro-10-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)carbonyl]dibenz[b,f][1,4]oxazepine STR30 A mixture of the product of Example 96 (37.0 g, 0.21 mole), n-<strong>[599-91-7]propyl tosylate</strong> (68.1 g, 0.31 mole), Na2 CO3 (16.8 g, 0.16 mole), and 160 mL of EtOH were refluxed for 14 hours under N2. After cooling the reaction, it was filtered and all solvent was removed from the filtrate under reduced pressure. The residue was mixed with 300 mL of water and extracted with 2*200 mL of Et2 O. The product HCl salt was precipitated and converted to hexahydro-1-propyl-1H-1,4-diazacycloheptane by the methods of Example 21.
 

Historical Records

Categories