Welcome to LookChem.com Sign In|Join Free
  • or
2-phenyl-2-phenylethynyl-1,3-indandione is a complex organic chemical compound characterized by a unique molecular structure. It features a 1,3-indandione core, which is a type of dione with a fused indane ring. The molecule is further distinguished by the presence of two phenyl groups and a phenylethynyl group, which are attached to the indandione core. 2-phenyl-2-phenylethynyl-1,3-indandione is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its structural diversity and reactivity. The specific arrangement of these functional groups endows the molecule with distinct chemical properties, making it a subject of interest in organic chemistry and drug development.

1483-86-9

Post Buying Request

1483-86-9 Suppliers

Recommended suppliers

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

1483-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1483-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1483-86:
(6*1)+(5*4)+(4*8)+(3*3)+(2*8)+(1*6)=89
89 % 10 = 9
So 1483-86-9 is a valid CAS Registry Number.

1483-86-9Relevant academic research and scientific papers

Reaction of alkynyl(phenyl)(p-phenylene)bisiodonium ditriflates with nucleophiles. High reactivity of the alkynyl component

Kitamura, Tsugio,Fukuoka, Takahiro,Zheng, Lei,Fujimoto, Takeshi,Taniguchi, Hiroshi,Fujiwara, Yuzo

, p. 2649 - 2654 (1996)

Reaction of alkynyl (p-phenylene) bisiodonium ditriflates with potassium thiocyanate in DMF gave alkynyl thiocyanates and p-iodophenyl (phenyl) iodonium triflate. The latter was readily removed by washing with water. The exclusive sulfur attack of thiocya

A novel hypervalent iodine reagent prepared from o-iodosylbenzoic acid and trifluoromethanesulfonic acid preparation and reactions of alkynyl(o-carboxyphenyl)iodonium triflates

Kitamura, Tsugio,Nagata, Kensuke,Taniguchi, Hiroshi

, p. 1081 - 1084 (2007/10/02)

A hyervalent iodine reagent prepared from o-iodosylbenzoic acid and trifluoromethanesulfonic acid (TfOH) (1:2) showed a high reactivity toward aromatic substrates, giving aryl(o-carboxyphenyl)iodonium triflates in good to high yields. Treatment of the iodine reagent with 1-trimethylsilylalkynes afforded alkynyliodonium triflates bearing carboxy group in high yields. The alkynyliodonium triflates indicated a high efficiency as a Michael acceptor to nucleophiles and the o-carboxyphenyliodonio group behaved as a good leaving group.

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 1483-86-9