Home Cart Sign in  
Chemical Structure| 39979-08-3 Chemical Structure| 39979-08-3
Chemical Structure| 39979-08-3

*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

CAS No. :39979-08-3
Formula : C8H17NO2
M.W : 159.23
SMILES Code : O=C(OC)CCCCCCN
MDL No. :MFCD08449741
InChI Key :AZRQWZVPEAHOOA-UHFFFAOYSA-N
Pubchem ID :11084159

Safety

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis

* 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 [ 39979-08-3 ]

[ 39979-08-3 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 10241-97-1 ]
  • [ 39979-08-3 ]
  • 7-[(5-methyl-1<i>H</i>-indole-2-carbonyl)-amino]-heptanoic acid methyl ester [ No CAS ]
  • 2
  • [ 39979-08-3 ]
  • [ 244090-34-4 ]
  • 7-[(1-phenyl-1<i>H</i>-indole-3-carbonyl)-amino]-heptanoic acid methyl ester [ No CAS ]
  • 3
  • [ 39979-08-3 ]
  • [ 27018-76-4 ]
  • 7-[(1-benzyl-1<i>H</i>-indole-3-carbonyl)-amino]-heptanoic acid methyl ester [ No CAS ]
  • 4
  • [ 58421-80-0 ]
  • [ 39979-08-3 ]
  • C17H23N3O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In isopropyl alcohol; at 90℃; for 6h; General procedure: 4-chloroqui nazoline analogues 3a-3j (10 mmol) and methyl 6-aminocaproate or methyl 7-aminoheptoate (11mmol) are dissolved in 30ml isopropanol and further added with 4 ml triethylamine. The reaction mixture is reacted under reflux for 6h followed by cooling to room temperature, and then added with a proper amount of water and extracted with ethyl acetate three times. The ethyl acetate layer is collected, dried over anhydrous Na2S04 and then concentrated under reduced pressure to get ester intermediates 4a-4l without further purification.
  • 5
  • [ 58421-80-0 ]
  • [ 39979-08-3 ]
  • N-hydroxy-7-((8-methylquinazolin-4-yl)amino)heptanamide [ No CAS ]
  • 6
  • [ 39979-08-3 ]
  • [ 16499-62-0 ]
  • 7-((7-fluoroquinazolin-4-yl)amino)-N-hydroxyheptanamide [ No CAS ]
  • 7
  • [ 39979-08-3 ]
  • [ 16499-62-0 ]
  • C16H20FN3O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In isopropyl alcohol; at 90℃; for 6h; General procedure: 4-chloroqui nazoline analogues 3a-3j (10 mmol) and methyl 6-aminocaproate or methyl 7-aminoheptoate (11mmol) are dissolved in 30ml isopropanol and further added with 4 ml triethylamine. The reaction mixture is reacted under reflux for 6h followed by cooling to room temperature, and then added with a proper amount of water and extracted with ethyl acetate three times. The ethyl acetate layer is collected, dried over anhydrous Na2S04 and then concentrated under reduced pressure to get ester intermediates 4a-4l without further purification.
 

Historical Records

Technical Information

Categories