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3976-29-2

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3976-29-2 Usage

Description

2-Propanol-1,1,1,3,3,3-d6, also known as deuterated isopropanol, is a variant of 2-propanol with the hydrogen atoms on the –CH3 groups replaced by deuterium. It is synthesized by the reduction of per-deuterioacetone and exists in both anti and gauche conformations. This deuterated compound has unique properties due to the presence of deuterium, which can be advantageous in various applications.

Uses

Used in Chemical Synthesis:
2-Propanol-1,1,1,3,3,3-d6 is used as a synthetic building block for the creation of complex deuterated compounds. The incorporation of deuterium atoms can provide specific isotopic effects that are beneficial for the study of reaction mechanisms, the development of new materials, and the synthesis of isotopically labeled compounds for various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Propanol-1,1,1,3,3,3-d6 can be utilized as a starting material for the synthesis of deuterated drug molecules. These deuterated drugs may exhibit improved pharmacokinetic properties, such as enhanced solubility, increased metabolic stability, and reduced toxicity, leading to better therapeutic outcomes.
Used in Analytical Chemistry:
2-Propanol-1,1,1,3,3,3-d6 can be employed as an internal standard or a reference compound in analytical chemistry. The presence of deuterium atoms allows for accurate quantification and identification of target molecules in complex mixtures, particularly in techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.
Used in Material Science:
In material science, 2-Propanol-1,1,1,3,3,3-d6 can be used to synthesize deuterated polymers and other materials with altered physical and chemical properties. These deuterated materials may exhibit improved mechanical strength, thermal stability, or chemical resistance, making them suitable for specific applications in various industries.
Used in Research and Development:
2-Propanol-1,1,1,3,3,3-d6 is a valuable compound for research and development purposes, particularly in the fields of organic chemistry, biochemistry, and materials science. It can be used to study the effects of deuterium substitution on molecular properties, reaction rates, and the behavior of compounds in different environments.

Check Digit Verification of cas no

The CAS Registry Mumber 3976-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3976-29:
(6*3)+(5*9)+(4*7)+(3*6)+(2*2)+(1*9)=122
122 % 10 = 2
So 3976-29-2 is a valid CAS Registry Number.

3976-29-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
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  • Aldrich

  • (392898)  2-Propanol-1,1,1,3,3,3-d6  99 atom % D

  • 3976-29-2

  • 392898-1G

  • 1,339.65CNY

  • Detail
  • Aldrich

  • (392898)  2-Propanol-1,1,1,3,3,3-d6  99 atom % D

  • 3976-29-2

  • 392898-5G

  • 3,100.50CNY

  • Detail

3976-29-2Relevant articles and documents

Air-stable iron catalyst for the Oppenauer-type oxidation of alcohols

Moyer, Sara A.,Funk, Timothy W.

scheme or table, p. 5430 - 5433 (2010/10/20)

An alcohol oxidation process using an air-stable iron tricarbonyl compound structurally similar to Shvo's diruthenium bridging hydride was developed. Secondary benzylic and allylic alcohols are oxidized in high yields, and evidence for an Oppenauer-type mechanism is presented.

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