7329-50-2 Usage
Description
PHENOL-2,4,6-D3,OD is a deuterated derivative of phenol, a type of organic compound that contains a hydroxyl group (-OH) bonded to an aromatic hydrocarbon. It is characterized by the presence of three deuterium atoms (D) at the 2nd, 4th, and 6th positions of the phenol ring, and an additional deuterium atom (OD) attached to the hydroxyl group. PHENOL-2,4,6-D3,OD is commonly used in various scientific and industrial applications due to its unique properties.
Uses
1. Used in Molecular Genetics Applications:
PHENOL-2,4,6-D3,OD is used as a stable isotope-labeled compound for molecular genetics applications. The incorporation of deuterium atoms in the molecule allows for the study of its behavior and interactions in biological systems, providing valuable insights into the mechanisms of genetic processes.
2. Used in the Synthesis of Antioxidant Compounds:
PHENOL-2,4,6-D3,OD is used as a starting material for the synthesis of antioxidant compounds. The phenol moiety in the molecule contributes to its antioxidant activity, making it a suitable candidate for the development of new antioxidants that can be used in various industries, such as pharmaceuticals, cosmetics, and the food industry.
3. Used in the Synthesis of Anti-Bacterial and Anti-Carcinogenic Compounds:
The unique structure of PHENOL-2,4,6-D3,OD allows it to be used in the synthesis of anti-bacterial and anti-carcinogenic compounds. The deuterated phenol ring can be further modified and functionalized to create new compounds with potential applications in the medical field, particularly in the development of novel antibiotics and anti-cancer drugs.
4. Used in the Food Industry:
PHENOL-2,4,6-D3,OD can be used in the food industry as a component in the synthesis of natural antioxidants. These antioxidants can be added to the food products to extend their shelf life, maintain their quality, and protect them from oxidation and spoilage.
5. Used in the Pharmaceutical Industry:
PHENOL-2,4,6-D3,OD can be utilized in the pharmaceutical industry for the development of new drugs with anti-bacterial, anti-carcinogenic, and antioxidant properties. The deuterated phenol structure can be a valuable building block for the synthesis of novel drug candidates that can be used to treat various diseases and conditions.
6. Used in the Cosmetics Industry:
In the cosmetics industry, PHENOL-2,4,6-D3,OD can be used as a key component in the development of antioxidant formulations. These formulations can be incorporated into various cosmetic products, such as creams, lotions, and serums, to provide protection against oxidative stress and promote skin health.
7. Used in the Agricultural Industry:
PHENOL-2,4,6-D3,OD can be employed in the agricultural industry for the synthesis of natural antioxidants that can be used to protect crops from oxidative damage caused by environmental stressors, such as UV radiation, temperature fluctuations, and pests. These antioxidants can also be used to extend the shelf life of harvested produce and maintain their quality during storage and transportation.
Check Digit Verification of cas no
The CAS Registry Mumber 7329-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7329-50:
(6*7)+(5*3)+(4*2)+(3*9)+(2*5)+(1*0)=102
102 % 10 = 2
So 7329-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H/i1D,4D,5D
7329-50-2Relevant articles and documents
Copper-catalysed low-temperature water-gas shift reaction for selective deuteration of aryl halides
Bartling, Stephan,Beller, Matthias,Bourriquen, Florian,Junge, Kathrin,Li, Wu,Liu, Weiping,Qu, Ruiyang,Rockstroh, Nils
, p. 14033 - 14038 (2021/11/12)
The introduction of deuterium atoms into organic compounds is of importance for basic chemistry, material sciences, and the development of drugs in the pharmaceutical industry, specifically for identification and quantification of metabolites. Hence, methodologies for the synthesis of selectively labelled compounds continue to be a major area of interest for many scientists. Herein, we present a practical and stable heterogeneous copper catalyst, which permits for dehalogenative deuterationviawater-gas shift reaction at comparably low temperature. This novel approach allows deuteration of diverse (hetero)aryl halides with good functional group tolerance, and no reduction of the aromatic rings or other easily reducible formyl and cyano groups. Multi-gram experiments show the potential of this method in organic synthesis and medicinal chemistry.
Shifted Selectivity in Protonation Enables the Mild Deuteration of Arenes through Catalytic Amounts of Bronsted Acids in Deuterated Methanol
Fischer, Oliver,Hubert, Anja,Heinrich, Markus R.
, p. 11856 - 11866 (2020/10/23)
Taking advantage of the "differentiating effect"of the solvent methanol, deuterations of electron-rich aromatic systems can be carried out under mild acid catalysis and thus under far milder conditions than known so far. The exceptional functional group t
A simple and cost-effective method for the regioselective deuteration of phenols
Zhan, Miao,Xu, Ruixue,Tian, Ye,Jiang, Hongxia,Zhao, Lifeng,Xie, Yongmei,Chen, Yuanwei
supporting information, p. 3370 - 3373 (2015/05/20)
A highly effective and operationally simple method for the deuteration of phenols using NaOH as a catalyst and D2O as the deuterium source is presented. A high regioselectivity for the ortho and/or para hydrogens relative to the oxygen atom was
