Welcome to LookChem.com Sign In|Join Free
  • or
α,2',5'-Trimethylacrylophenone is an organic compound with the chemical formula C12H14O. It is a derivative of acrylophenone, featuring a phenyl ring with three methyl groups attached at the α, 2', and 5' positions, and an acrylic group (CH2=CHCO) at the α position. α,2',5'-Trimethylacrylophenone is known for its potential applications in the synthesis of various chemical products, such as dyes and pharmaceuticals, due to its reactive functional groups. It is typically synthesized through chemical reactions involving acrylophenone and methylating agents. As with many organic compounds, it is important to handle α,2',5'-trimethylacrylophenone with care, as it may have specific safety and environmental considerations.

16205-96-2

Post Buying Request

16205-96-2 Suppliers

Recommended suppliers

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

16205-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16205-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16205-96:
(7*1)+(6*6)+(5*2)+(4*0)+(3*5)+(2*9)+(1*6)=92
92 % 10 = 2
So 16205-96-2 is a valid CAS Registry Number.

16205-96-2Relevant academic research and scientific papers

PROTEIN CROSSLINKING INHIBITOR AND USE OF THE SAME

-

Page/Page column 28, (2012/11/08)

The present invention relates to: a ketone compound having transglutaminase-inhibiting activity, which is represented by the following Formula 1, 2, or 3: wherein R1 is a substituted or unsubstituted aryl or heterocyclyl group, R2, R3, and R4 are hydrogen atoms, n is 2, X is halogen, R5 and R6 independently represent a hydrogen atom or a substituted or unsubstituted C1-C10 alkyl, aryl, or aralkyl group, wherein R5 and R6 are not hydrogen atoms at the same time, or R5 and R6 may be taken together to form a saturated or unsaturated and substituted or unsubstituted heterocyclyl group containing a nitrogen atom (N); an inhibitor of protein crosslinking comprising the compound; and a composition for preventing or treating a protein-crosslinking causative disease, which comprises the compound or the protein crosslinking inhibitor.

Photoenolization-induced oxirane ring opening in 2,5-dimethylbenzoyl oxiranes to form pharmaceutically promising indanone derivatives

Solomek, Tomas,Stacko, Peter,Tazhe Veetil, Aneesh,Pospisil, Tomas,Klan, Petr

experimental part, p. 7300 - 7309 (2011/01/12)

Irradiation of 2,5-dimethylbenzoyl oxiranes results in a relatively efficient and high-yielding formation of β-hydroxy functionalized indanones that structurally resemble biologically active pterosines. Nanosecond laser flash photolysis and quantum-chemical calculations based on density functional theory provided evidence that this photochemical transformation proceeds primarily via a photoenolization mechanism. Our study revealed considerable complexity of the mechanism and that structural modifications can significantly alter the reaction pathway and yield different products. The scope of this photochemical transformation for the synthesis of some pharmaceutically important compounds was investigated.

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 16205-96-2