Home Cart Sign in  
Chemical Structure| 5142-75-6 Chemical Structure| 5142-75-6

Structure of 5142-75-6

Chemical Structure| 5142-75-6

*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 [ 5142-75-6 ]

CAS No. :5142-75-6
Formula : C21H21Bi
M.W : 482.37
SMILES Code : CC1=CC=C([Bi](C2=CC=C(C)C=C2)C3=CC=C(C)C=C3)C=C1
MDL No. :MFCD00123272

Safety of [ 5142-75-6 ]

Application In Synthesis of [ 5142-75-6 ]

* 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 [ 5142-75-6 ]

[ 5142-75-6 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 120-35-4 ]
  • [ 5142-75-6 ]
  • 3-(4-Methyl-phenylamino)-4-methoxy-N-phenyl-benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine;copper diacetate; Example 34 3-(4-Methyl-phenylamino)-4-methoxy-N-phenyl-benzamide Prepared according to the procedure of Example 25 using 3-amino-4-methoxy-N-phenyl-benzamide (1.1 g, 4.5 mmol), tris(4-methylphenyl)bismuthine (2.5 g, 5.2 mmol), copper(II) acetate (0.82 g, 4.5 mmol), and triethylamine (0.46 g, 4.5 mmol) to afford the product (0.8 g); m.p. 187-188 C. after recrystallization from acetonitrile then ethyl acetate. Calculated for C21H20N2O2: C, 75.88; H, 6.06; N, 8.43. Found: C, 75.57; H, 5.83; N, 8.34.
  • 3
  • [ 17024-12-3 ]
  • [ 7787-58-8 ]
  • [ 5142-75-6 ]
  • bis(4-methylphenyl)(9-phenanthryl)bismuthane [ No CAS ]
  • 4
  • [ 4181-20-8 ]
  • [ 5142-75-6 ]
  • [ 138689-62-0 ]
  • 5
  • [ 19063-55-9 ]
  • [ 5142-75-6 ]
  • [ 1259294-15-9 ]
YieldReaction ConditionsOperation in experiment
81% With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; triphenylphosphine; cesium fluoride; In N,N-dimethyl-formamide; at 90℃; for 1h;Inert atmosphere; Green chemistry; General procedure: Under inert atmosphere (N2), in a 25 mL round bottom flask, Ar3Bi (0.208 mmol; 0.35 eq.), CsF (0.24 g: 1.8 mmol; 3 eq.), PPh3 (0.004 g: 0.018 mmol; 3 mol%), the aryl bromide (0.60 mmol; 1 eq.) was added to DMF (5 mL). The solution was warmed to 90 C prior addition of PEPPSI IPr (0.012 g: 0.018 mmol; 3 mol%). The reaction was monitored by GC/MS to follow the total consumption of the aryl bromide. Cooled to room temperature (RT), the reaction mixture was diluted by addition of diethyl ether (20 mL) and aqueous HCl 6 M (30 mL). After decantation, the aqueous solution was extracted with diethylether (2 * 20 mL). The collected organic phases were then washed with HCl 6 N (2 * 25 mL), water (25 mL) and brine (25 mL) prior drying over MgSO4. After concentration under reduced pressure, the resulting crude product was subjected to purification by column chromatography leading after concentration under reduced pressure to the title compound.
  • 6
  • [ 95-16-9 ]
  • [ 5142-75-6 ]
  • [ 16112-21-3 ]
  • 7
  • [ 149-30-4 ]
  • [ 5142-75-6 ]
  • [ 16112-21-3 ]
YieldReaction ConditionsOperation in experiment
98% With copper diacetate; bis(dibenzylideneacetone)-palladium(0); In N,N-dimethyl-formamide; at 80℃; for 3h;Inert atmosphere; General procedure: A mixture of azole-2-thione (1a-k, 0.5 mmol), triarylbismuthine (2a-k, 0.5 mmol, 1.0 eq), Cu(OAc)2 (182 mg, 1.0 mmol, 2.0 eq), Pd(dba)2 (28.8 mg, 0.05 mmol, 10 mol%) in DMF (3.0 mL) was heated 80 C under argon atmosphere for 3 hr. After the reaction complete, the mixture was allowed to cool to room temperature. The reaction mixture solution was purified by column chromatography on silica gel without work up. The products were characterized based on their physical and spectral data.
 

Historical Records