Home Cart Sign in  
Chemical Structure| 834881-64-0 Chemical Structure| 834881-64-0

Structure of 834881-64-0

Chemical Structure| 834881-64-0

*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 [ 834881-64-0 ]

CAS No. :834881-64-0
Formula : C13H21N3O2
M.W : 251.33
SMILES Code : O=C(OC(C)(C)C)NCCNC1=CC=CC=C1N
MDL No. :MFCD09800564

Safety of [ 834881-64-0 ]

Application In Synthesis of [ 834881-64-0 ]

* 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 [ 834881-64-0 ]

[ 834881-64-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1003-61-8 ]
  • [ 834881-64-0 ]
  • tert-butyl 2-(2-(2-aminothiazol-5-yl)-1H-benzo[d]imidazol-1-yl)ethylcarbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
14% at 110℃; for 4h;Inert atmosphere; Prepared from tert-butyl 2-(2-aminophenylamino)ethylcarbamate (24; 0.126 g, 0.50 mmol), <strong>[1003-61-8]2-aminothiazole-5-carbaldehyde</strong> (0.070 g, 0.55 mmol), and PEG-400 (0.125 mL) using a reaction temperature of 110 C. After cooling, the crude reaction mixture was dissolved in ethyl acetate (3 mL), and water (3 mL) was added. Upon shaking, a light orange precipitate formed. This precipitate was isolated by filtration and then washed with ethyl acetate (3 mL) and chloroform (3 mL). The solid was air dried and then taken up in DMF and purified by preparative HPLC chromatography (Method 1) to give 22c (0.024 g, 14%) as an off-white solid.
 

Historical Records

Technical Information

Categories