Home Cart Sign in  
Chemical Structure| 58464-25-8 Chemical Structure| 58464-25-8

Structure of 58464-25-8

Chemical Structure| 58464-25-8

*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 [ 58464-25-8 ]

CAS No. :58464-25-8
Formula : C16H18IN
M.W : 351.23
SMILES Code : C[N+]1=C(C)C(C)(C)C2=C1C=CC3=CC=CC=C23.[I-]
MDL No. :MFCD00142374

Safety of [ 58464-25-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 58464-25-8 ]

* 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 [ 58464-25-8 ]

[ 58464-25-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24372-46-1 ]
  • [ 58464-25-8 ]
  • (E)-2-(2-(5-(dimethylamino)thiophen-2-yl)vinyl)-1,1,3-trimethyl-1H-benzo-[e]indol-3-ium iodide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With piperidine; In ethanol; at 85℃; for 12.0h; Take 0.5g of 4-dimethylaminothiophene-2-carboxaldehyde and the corresponding mass of 1,1,2,3-tetramethyl-1H-benzo[e]indolium iodide (The molar ratio of the two is 1.1:1). Add to 20mL of absolute ethanol. 2 to 3 drops of piperidine were added dropwise as a catalyst, and the mixture was refluxed at 85 C for 12 hours; after completion of the reaction, it was cooled to room temperature, and most of the solvent was removed by rotary evaporation. Then, it was poured into diethyl ether and precipitated, and the product was obtained by filtration. After drying, it is recrystallized several times with ethanol. vacuum drying, obtain (E)-2-(2-(5-(dimethylamino)thiophen-2-yl)vinyl)-1,1,3-trimethyl-1H-benzo[e]indolium iodide.
  • 2
  • [ 2243-58-5 ]
  • [ 58464-25-8 ]
 

Historical Records

Categories