Welcome to LookChem.com Sign In|Join Free
  • or
3-(4-chlorophenyl)-4,5,6,7-tetrahydrobenzisoxazole is a chemical compound with the molecular formula C11H12ClNO2. It is a derivative of benzisoxazole, a heterocyclic compound consisting of a benzene ring fused to an isoxazole ring. The compound features a 4-chlorophenyl group attached to the benzene ring, which imparts unique chemical and physical properties. 3-(4-chlorophenyl)-4,5,6,7-tetrahydrobenzisoxazole is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its structural diversity and the presence of a chlorine atom, which can be used for further functionalization.

61054-28-2

Post Buying Request

61054-28-2 Suppliers

Recommended suppliers

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

61054-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61054-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,5 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61054-28:
(7*6)+(6*1)+(5*0)+(4*5)+(3*4)+(2*2)+(1*8)=92
92 % 10 = 2
So 61054-28-2 is a valid CAS Registry Number.

61054-28-2Downstream Products

61054-28-2Relevant academic research and scientific papers

Palladium-Catalyzed Direct C-H Arylation of Isoxazoles at the 5-Position

Shigenobu, Masashi,Takenaka, Kazuhiro,Sasai, Hiroaki

supporting information, p. 9572 - 9576 (2015/08/11)

A palladium-catalyzed direct arylation of isoxazoles with aryl iodides has been achieved. The C-H bond at the 5-position is activated selectively to give coupling products in moderate to good yields. This direct arylation was applied to the synthesis of a spiro-type chiral ligand, which proved to be most effective to the palladium-catalyzed tandem cyclization of a dialkenyl alcohol.

SYNTHESIS OF ISOXAZOLE DERIVATIVES IN REACTION OF 2-HYDROXYPHENYLCARBONYL COMPOUNDS OR 1,3-DIKETONES WITH HYDROXYLAMINE-O-SULFONIC ACID

Suwinski, J.,Walczak, K.

, p. 777 - 785 (2007/10/02)

2-Hydroxybenzaldehyde 1a and 2-hydroxyacetophenone 1b react with hydroxylamine-O-sulfonic acid (HSA) yielding the corresponding oxime hydrogensulfates 2a and 2b, separated as potassium salts.These salts undergo conversion with good yields to benzisoxazole 3a and 2-methylbenzoxazole 3b, respectively.In similar reaction of 1,3-diketones, both cyclic and acyclic 1c-k with HSA, isoxazole derivatives 3c-k were obtained.

Synthesis of Isomeric Series of Aryltetrahydrobenzisoxazoles and Arylcyclopentisoxazoles

Fos, Empar,Borras, Liset,Gasull, Maria,Mauleon, David,Carganico Germano

, p. 203 - 208 (2007/10/02)

Four series of potential PAF-antagonists in which the isoxazole nucleus is condensed with a polyhydrogenated five- or six-carbon ring were prepared.The synthesis of the compounds 3-aryl-4,5,6,7-tetrahydrobenzisoxazoles 1, 3-arylcyclopentisoxazole 2,

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 61054-28-2