Home Cart Sign in  
Chemical Structure| 32002-72-5 Chemical Structure| 32002-72-5

Structure of 32002-72-5

Chemical Structure| 32002-72-5

*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 [ 32002-72-5 ]

CAS No. :32002-72-5
Formula : C11H9NO2S
M.W : 219.26
SMILES Code : O=C(C1=C(C2=CC=CC=C2)N=C(C)S1)O
MDL No. :MFCD07348569

Safety of [ 32002-72-5 ]

Application In Synthesis of [ 32002-72-5 ]

* 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 [ 32002-72-5 ]

[ 32002-72-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32002-72-5 ]
  • [ 525-03-1 ]
  • 1-(9H-fluoren-9-yl)-3-(2-methyl-4-phenyl-1,3-thiazol-5-yl)urea [ No CAS ]
YieldReaction ConditionsOperation in experiment
COMPOUND 2 l-(9H-Fluoren-9-yl)-3-(2-methyl-4-phenylthiazol-5-yl)urea To a solution of 2-methyl-4-phenyl-l,3-thiazole-5-carboxylic acid (20 mg, 0.091 mmol) and diphenylphosphorylazide (28 mg, 0.10 mmol) in toluene (1 mL) was added TEA (0.025 mL, 0.18 mmol). The resulting mixture was stirred at 23 C for 1 h and then heated at reflux for 1 h. The reaction mixture was cooled to 23 C and a solution of 9H-fluoren-9-amine (16 mg, 0.091 mmol) in toluene (1 mL) was added. The resulting mixture was stirred for 16 h at 23 C, then concentrated. The residue was purified by prep-HPLC (5-95% acetonitrile + 0.1% trifluoroacetic acid in water) to give the title compound. MS : m/z = 381.1 (M+H). 1H NMR (500 MHz, DMSO): δ 8.72 (s, 1 H); 7.86 (d, / = 7.6 Hz, 2 H); 7.65 (d, / = 7.7 Hz, 2 H); 7.59 (d, / = 7.5 Hz, 2 H); 7.41-7.45 (m, 4 H); 7.29-7.37 (m, 4 H); 5.86 (d, / = 8.0 Hz, 1 H); 2.58 (s, 3 H).
To a solution of 2-methyl-4-phenyl-l,3-thiazole-5-carboxylic acid (20 mg, 0.091 mmol) and diphenylphosphorylazide (28 mg, 0.10 mmol) in toluene (1 mL) was added TEA (0.025 mL, 0.18 mmol). The resulting mixture was stirred at 23 C for 1 h and then heated at reflux for 1 h. The reaction mixture was cooled to 23 C and a solution of 9H-fluoren-9-amine (16 mg, 0.091 mmol) in toluene (1 mL) was added. The resulting mixture was stirred for 16 h at 23 C, then concentrated. The residue was purified by prep-HPLC (5-95% acetonitrile + 0.1% trifluoroacetic acid in water) to give the title compound. MS: mlz = 381.1 (M+H). NMR (500 MHz, DMSO): δ 8.72 (s, 1 H); 7.86 (d, J= 7.6 Hz, 2 H); 7.65 (d, J= 7.7 Hz, 2 H); 7.59 (d, J= 7.5 Hz, 2 H); 7.41-7.45 (m, 4 H); 7.29-7.37 (m, 4 H); 5.86 (d, J= 8.0 Hz, 1 H); 2.58 (s, 3 H).
 

Historical Records

Technical Information

Categories