Home Cart Sign in  
Chemical Structure| 23596-28-3 Chemical Structure| 23596-28-3

Structure of 23596-28-3

Chemical Structure| 23596-28-3

*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 of [ 23596-28-3 ]

CAS No. :23596-28-3
Formula : C7H8N2
M.W : 120.15
SMILES Code : C12=C(NCC2)C=CN=C1
MDL No. :MFCD18382584

Safety of [ 23596-28-3 ]

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

Application In Synthesis of [ 23596-28-3 ]

* 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 [ 23596-28-3 ]

[ 23596-28-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 271-34-1 ]
  • [ 23596-28-3 ]
YieldReaction ConditionsOperation in experiment
41% With hydrogen;Raney nickel; In ethanol; at 70℃; under 2250.23 Torr; for 72h; Step 3: 2,3-dihydro-1H-pyrrole[3,2-c]pyridine 1.5 g (12.7 mmol) 1H-pyrrole[3,2-c]pyridine in 70 mL EtOH were combined with 0.75 g Raney nickel and hydrogenated for 3 days at 70 C. in a 3 bar hydrogen atmosphere. The catalyst was removed by suction filtering and the filtrate was evaporated down. The residue was purified by flash chromatography. The product-containing fractions were combined and evaporated down. Yield: 0.62 g (41% of theoretical) ESI-MS: m/z=121 (M+H)+ Rf: 0.12 (silica gel, DCM/MeOH/NH4OH 80:20:2)
41% With hydrogen; In ethanol; at 70℃; under 2250.23 Torr; for 72h; 2,3-dihydro-1H-pyrrolo[3,2-c]pyridine 1.50 g (12.7 mmol) <strong>[271-34-1]5-azaindole</strong> and 0.75 g Raney nickel in 70 mL ethanol were hydrogenated in a hydrogen atmosphere at 3 bar hydrogen pressure for 3 days at 70 C. Then the catalyst was suction filtered and the solution was evaporated down i. vac. The residue was purified through a silica gel column. The product fractions were combined and evaporated down using the rotary evaporator. Yield: 620 mg (41% of theoretical) ESI-MS: m/z=121 (M+H)+
 

Historical Records

Categories