Welcome to LookChem.com Sign In|Join Free
  • or
ethyl 4-acetyl-1-(4-bromophenyl)-5-methyl-1H-pyrazole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96734-86-0

Post Buying Request

96734-86-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

96734-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96734-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,3 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96734-86:
(7*9)+(6*6)+(5*7)+(4*3)+(3*4)+(2*8)+(1*6)=180
180 % 10 = 0
So 96734-86-0 is a valid CAS Registry Number.

96734-86-0Relevant academic research and scientific papers

In Situ Generation of Nitrilimines from Aryldiazonium Salts and Diazo Esters: Synthesis of Fully Substituted Pyrazoles under Room Temperature

Shao, Ying,Zheng, Hao,Qian, Junfeng,Wan, Xiaobing

supporting information, p. 2412 - 2415 (2018/04/27)

A novel one-pot synthesis for fully substituted pyrazoles has been well developed via the in situ generation of nitrilimines from aryldiazonium salts and diazo esters and a subsequent cycloaddition with 1,3-dicarbonyl compounds. High yields, mild conditio

1,3-Dipolar Cycloaddition of Four Hydrazonoyl Chlorides to β-Diketones and α,β-Unsaturated Ketones

Albar, Hassan A.

, p. 872 - 889 (2007/10/03)

The 1,3-dipolar cycloaddition of four hydrazonoyl chloride derivatives with the sodium salt of unsymmetrical β-diketones (benzoylacetone) offers a versatile method for the regioselective synthesis of 2H-pyrazoles in a similar fashion to the cycloaddition of the nitrilimides with α,β-unsaturated ketones and esters. The structures of the prepared isomeric pyrazole and pyrazoline derivatives were established by spectroscopic and chemical methods.

The Regioselectivity of the 1,3-Dipolar Cycloaddition of α-Carbonylformonitrile N-arylimides To Benzylideneacetone and β-Diketones

Albar, Hassan A.

, p. 1756 - 1764 (2007/10/03)

The cycloaddition of the ethoxycarbonylformonitrile N-arylimides 2 to benzylideneacetone afforded two regioisomers, 5-acetyl- and 4-acetyl-dihydropyrazole but the cycloaddition of 2 to benzoylacetone afforded two regioisomers, 4-acetyl- and 4-benzoylpyrazole.Also, some pyrazolopyridazin-7-one and pyrazolopyridazinderivatives were synthesized.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 96734-86-0