Home Cart Sign in  
Chemical Structure| 23758-95-4 Chemical Structure| 23758-95-4

Structure of 23758-95-4

Chemical Structure| 23758-95-4

*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 [ 23758-95-4 ]

CAS No. :23758-95-4
Formula : C10H11N
M.W : 145.20
SMILES Code : C12=CC=CC=C1C=NCCC2
MDL No. :MFCD26129881

Safety of [ 23758-95-4 ]

Application In Synthesis of [ 23758-95-4 ]

* 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 [ 23758-95-4 ]

[ 23758-95-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 271-34-1 ]
  • [ 23758-95-4 ]
  • 3-(2,3,4,5-tetrahydro-1H-benzo[c]azepin-1-yl)-5-azaindole [ No CAS ]
YieldReaction ConditionsOperation in experiment
65% With toluene-4-sulfonic acid; In neat (no solvent); at 100℃; for 3.5h;Microwave irradiation; the mixture of the cyclic imine 3,4-dihydroisoquinoline (66 mg, 0.50 mmol);6,7-dihydrothieno[3,2-c]pyridine (51 mg, 0.38 mmol); 3,4-dihydro--carboline (63 mg, 0.38 mmol) or4,5-dihydro-3H-benz[c]azepine (55.3 mg, 0.38 mmol); and the electron-rich aromatic compound (7-, 6-,4-, or <strong>[271-34-1]5-azaindole</strong> (30 mg, 0.25 mmol)) were placed in a 10 mL pressurized reaction vial and heated ina microwave reactor, under the conditions given in Tables 1-3. In the case of <strong>[271-34-1]5-azaindole</strong>, 10 mol % ofp-TSA (4.3 mg, 0.025 mmol) as a catalyst was also added.
 

Historical Records