Home Cart Sign in  
Chemical Structure| 13311-79-0 Chemical Structure| 13311-79-0

Structure of 13311-79-0

Chemical Structure| 13311-79-0

*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 [ 13311-79-0 ]

CAS No. :13311-79-0
Formula : C9H12N2O
M.W : 164.20
SMILES Code : COC1=CC2=C(NCCN2)C=C1
MDL No. :MFCD17171353
InChI Key :SXRFQDARJDXESM-UHFFFAOYSA-N
Pubchem ID :12549514

Safety of [ 13311-79-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 13311-79-0 ]

* 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 [ 13311-79-0 ]

[ 13311-79-0 ] Synthesis Path-Downstream   1~6

  • 3
  • [ 102-51-2 ]
  • [ 13311-79-0 ]
  • 5
  • [ 106-93-4 ]
  • [ 102-51-2 ]
  • [ 13311-79-0 ]
YieldReaction ConditionsOperation in experiment
35.3% With sodium hydrogencarbonate; In N,N-dimethyl acetamide; at 80℃; General procedure: 1,2-Dibromoethane (2.1 mL, 24 mmol) was added dropwise to a suspension of substituted ophenylenediamine derivative 1 (20 mmol) and NaHCO3(16.8g, 200 mmol) in dimethyl acetylamide (30mL) at 800 while stirring for 6-8 hr. The reaction mixture was cooled, filtered, washed thoroughly with NaCl aq, and dried over anhydrous Na2SO4. After concentration under reduced pressure, the residue was subjected to silica gel chromatography eluting with EtOAc-petroleum ether (PE) mixture (4:1) to get 2a-f.
  • 6
  • [ 79-36-7 ]
  • [ 13311-79-0 ]
  • 1,4-bis(dichloroacetyl)-6-methoxy-1,2,3,4-tetrahydroquinoxaline [ No CAS ]
YieldReaction ConditionsOperation in experiment
48.9% With sodium carbonate; In benzene; at 20 - 25℃; for 1.0h; General procedure: Dichloroacetyl chloride (2.4 mL, 24 mmol) was added dropwise to a suspension of 2 (10 mmol) and Na2CO3 (2.55g, 24 mmol) in benzene (30 ml) at room temp with stirring. The mixture was stirred continuously for 1 hr and then it was taken up in a mixture of water and EtOAc. The organic phase was washed with saturated NaCl aq, dried over anhyNa2SO4 and vacuum distillation gave the residue. Recrystallization of the residue with ethanol gave pure products 4a-f.
 

Historical Records

Technical Information

Categories