Welcome to LookChem.com Sign In|Join Free
  • or
2,4-dimethoxy-α-phenoxyacetophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20744-30-3

Post Buying Request

20744-30-3 Suppliers

Recommended suppliers

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

20744-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20744-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,4 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20744-30:
(7*2)+(6*0)+(5*7)+(4*4)+(3*4)+(2*3)+(1*0)=83
83 % 10 = 3
So 20744-30-3 is a valid CAS Registry Number.

20744-30-3Relevant academic research and scientific papers

Identification of a Novel Oxadiazole Inhibitor of Mammalian Target of Rapamycin

Lim, Sunwoo,Lee, Hyomin,Kim, Euijung,Hur, Wooyoung

, p. 296 - 303 (2020)

We performed a biochemical screen against mTOR using in-house small molecule library. Two novel, structurally distinct hits were identified. Among them, a novel oxadiazole scaffold compound (2) suppressed the phosphorylation of both S6K1 and Akt1 in HeLa cells. Docking study suggested that 2 is ATP-competitive and shows a pi-pi interaction with Trp2239 and hydrogen bonds with Trp2239 and Thr2245. Through derivatization, a slightly more potent analogue (2a) was identified with IC50 of 9.6 μM. Our study provides a starting point for discovery of novel potent mTOR inhibitors.

The reduction of α-X-acetophenones (X = PhO, Br, Cl) in hydrogendonating solvents at elevated temperatures

Dorrestijn, Edwin,Hemmink, Sven,Hulstman, Guido,Monnier, Laurent,Van Scheppingen, Wibo,Mulder, Peter

, p. 607 - 616 (2007/10/03)

The reduction of α-X-acetophenones (X = PhO, Br, Cl), as model compounds for lignin liquefaction studies, has been investigated in the presence of a hydrogen-donating solvent such as 9,10-dihydroanthracene (AnH2) or 2-propanol, between 373 and 573 K. With α-phenoxyacetophenone (PAP) in AnH2, acetophenone and phenol have been obtained with high selectivities. The mechanism involves the reverse radical disproportionation (RRD) with AnH2. Hydrodebromination of α-bromoacetophenone (BrAP) is quantitative at 423 K using AnH2 as a reducing agent. Now, the hydrogen transfer proceeds by an uninhibited radical chain mechanism with anthracenyl radicals as the chain carriers. For the kinetic analysis, the C-X (X = Br, Cl) bond dissociation enthalpies (BDEs) have been determined by means of very low pressure pyrolysis to give BDE(C-Br) = 271 kJ mol-1 and, as a lower limit, BDE(C-Cl) ? 309 kJ mol-1, at 298 K. The BDEs are quite at variance with recently published insights derived from an electrochemical study. For comparison, density functional theory calculations (DFT) have been performed.

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 20744-30-3