Welcome to LookChem.com Sign In|Join Free
  • or
3-chloro-benzoic acid 2-(3-chloro-benzoyl)-4-methyl-phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

794513-64-7

Post Buying Request

794513-64-7 Suppliers

Recommended suppliers

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

794513-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 794513-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,5,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 794513-64:
(8*7)+(7*9)+(6*4)+(5*5)+(4*1)+(3*3)+(2*6)+(1*4)=197
197 % 10 = 7
So 794513-64-7 is a valid CAS Registry Number.

794513-64-7Downstream Products

794513-64-7Relevant academic research and scientific papers

Synthesis of some newer analogues of substituted dibenzoyl phenol as potent anti-inflammatory agents

Khanum, Shaukath Ara.,D, Venu T.,Shashikanth, Sheena,Firdouse, Aiysha

, p. 5351 - 5355 (2004)

The newly synthesized compounds dibenzoyl phenols 4a-f using microwave irradiation were screened for their anti-inflammatory activity and compared with standard drugs. Benzoylation of hydroxybenzophenones 1a-f affords substituted benzoyl phenyl benzoates

Synthesis and crystallographic analysis of benzophenone derivatives-The potential anti-inflammatory agents

Venu,Shashikanth,Khanum,Naveen,Firdouse, Aiysha,Sridhar,Shashidhara Prasad

, p. 3505 - 3514 (2008/02/07)

Fries rearrangement of substituted phenyl benzoates 1a-j to substituted hydroxy benzophenones 2a-j was achieved in excellent yield. Further benzoylation of 2a-j to benzoyloxy benzophenones 4a-n, a benzophenone analogue was achieved in good yield. All the newly synthesized compounds were evaluated for their anti-inflammatory activity and were compared with standard drugs. Out of the compounds studied, the compounds 4c, 4e, 4g, 4h and 4k with chloro and methyl substituents at para position showed more potent activity than the standard drugs at all doses tested.

Synthesis of benzoyl phenyl benzoates as effective inhibitors for phospholipase A2 and hyaluronidase enzymes

Khanum, Shaukath Ara,Murari, Satish Kumar,Vishwanth, Bannikuppe Sannanaik,Shashikanth, Sheena

, p. 4100 - 4104 (2007/10/03)

Benzoylation of (hydroxy phenyl) phenyl methanone 2a-g to benzoyl phenyl benzoates 4a-g, a benzophenone analogue, was achieved in good yield. All the newly synthesized compounds were evaluated for their phospholipase A2 [E.C. 3.1.1.4] and hyaluronidase [E.C. 3.2.1.35] enzyme inhibitory activity in snake venom as source and their structure-activity relationship with respect to different groups is reported for the first time. The in vitro PLA2 enzyme inhibitory activity and in vivo anti-inflammatory activity studies of benzoyl phenyl benzoates are illustrated.

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 794513-64-7