Home Cart Sign in  
Chemical Structure| 26579-54-4 Chemical Structure| 26579-54-4

Structure of 26579-54-4

Chemical Structure| 26579-54-4

*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 [ 26579-54-4 ]

CAS No. :26579-54-4
Formula : C7H6N2S
M.W : 150.20
SMILES Code : NC1=CSC2=C1C=CC=N2
MDL No. :MFCD11869737

Safety of [ 26579-54-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 26579-54-4 ]

* 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 [ 26579-54-4 ]

[ 26579-54-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-85-0 ]
  • [ 872-50-4 ]
  • [ 111042-89-8 ]
  • [ 26579-54-4 ]
YieldReaction ConditionsOperation in experiment
4.94 g (86.0%) EXAMPLE 1 3-(1-Piperazinyl)thieno[2,3-b]pyridine maleate A mixture of <strong>[111042-89-8]3-aminothieno[2,3-b]pyridine-2-carboxylic acid methyl ester</strong> (8.00 g), piperazine (6.70 g), and N-methyl-2-pyrrolidinone (80 ml) was heated to 145 C. for 3 hr, under a nitrogen atmosphere. The solution was allowed to cool, diluted with water (400 ml), and extracted with ethyl acetate. The combined extracts were washed with water and brine dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to give 4.94 g (86.0%) of residual thieno[2,3-b]pyridine-3-amine.
 

Historical Records

Technical Information

Categories