70938-00-0 Usage
Description
1,3-Dihydroxybenzene-d6, also known as Resorcinol-d6, is a benzene derivative that is isotopically labeled with deuterium. It is structurally similar to resorcinol, which is a well-known compound with various applications in the pharmaceutical and chemical industries. The presence of deuterium in the molecule makes it particularly useful for research purposes, as it can be employed in various analytical techniques to study the behavior of the compound and its interactions with other molecules.
Uses
Used in Pharmaceutical Industry:
1,3-Dihydroxybenzene-d6 is used as a keratolytic and antiseborrheic agent for the treatment of skin conditions such as excessive dryness, scaling, and flaking. It helps to break down and remove the outer layer of dead skin cells, promoting a smoother and healthier skin appearance.
Used in Veterinary Medicine:
1,3-Dihydroxybenzene-d6 is used as a topical antipruritic and antiseptic in veterinary medicine. It helps to relieve itching and irritation caused by various skin conditions and also possesses antimicrobial properties, making it effective against bacterial infections.
Used in Research and Development:
1,3-Dihydroxybenzene-d6 is a valuable isotopically labeled research compound. It is used in various scientific studies to investigate the properties and behavior of resorcinol and its derivatives. The presence of deuterium in the molecule allows researchers to track its interactions with other molecules and study its metabolic pathways, which can be crucial for understanding its pharmacological effects and potential applications in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 70938-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,3 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70938-00:
(7*7)+(6*0)+(5*9)+(4*3)+(3*8)+(2*0)+(1*0)=130
130 % 10 = 0
So 70938-00-0 is a valid CAS Registry Number.
70938-00-0Relevant articles and documents
Stoichiometric and catalytic H/D incorporation by cationic iridium complexes: A common monohydrido-iridium intermediate
Yung, Cathleen M.,Skaddan, Marc B.,Bergman, Robert G.
, p. 13033 - 13043 (2004)
A mechanistic study of the Stoichiometric and catalytic H/D exchange reactions involving cationic iridium complexes is presented. Strong evidence suggests that both Stoichiometric and catalytic reactions proceed via a monohydrido-iridium species. Stoichiometric deuterium incorporation reactions introduce multiple deuterium atoms into the organic products when aryliridium compounds Cp*PMe3Ir(C6H4X)(OTf) (X = H, o-CH3, m-CH3, p-CH3) react with D2. Multiple deuteration occurs at the unhindered positions (para and meta) of toluene, when X = CH3. The multiple-deuteration pathway is suppressed in the presence of an excess of the coordinating ligand, CH3CN. The compound Cp*PMe3IrH(OTf) (1-OTf) is observed in low-temperature, Stoichiometric experiments to support a monohydrido-iridium intermediate that is responsible for catalyzing multiple deuteration in the stoichiometric system. When paired with acetone-d6, [Cp*PMe3IrH3][OTf] (4) catalytically deuterates a wide range of substrates with a variety of functional groups. Catalyst 4 decomposes to [Cp*PMe3Ir(η3-CH 2C(OH)CH2)][OTf] (19) in acetone and to [Cp*PMe 3IrH(CO)]-[OTf] (1-CO) in CH3OH. The catalytic H/D exchange reaction is not catalyzed by simple H+ transfer, but instead proceeds by a reversible C-H bond activation mechanism.
