51326-51-3 Usage
Description
4-TETRAHYDROPYRANYLOXY-BUTAN-1-OL, also known as a Tetrahydropyranyl (THP) ether, is a colorless oil with useful chemical properties. It is a versatile building block in the synthesis of various organic compounds due to its ability to protect alcohols and other functional groups during chemical reactions.
Uses
Used in Pharmaceutical Industry:
4-TETRAHYDROPYRANYLOXY-BUTAN-1-OL is used as a protecting group for alcohols in the pharmaceutical industry. Its application is crucial for preventing unwanted side reactions and ensuring the selective functionalization of specific groups in complex organic molecules, ultimately leading to the desired drug candidates.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-TETRAHYDROPYRANYLOXY-BUTAN-1-OL is used as a versatile building block for the creation of various organic compounds. Its ability to protect alcohols and other functional groups allows chemists to carry out selective reactions, leading to the formation of target molecules with high purity and yield.
Used in Research and Development:
4-TETRAHYDROPYRANYLOXY-BUTAN-1-OL is also utilized in research and development for the synthesis of novel compounds with potential applications in various fields, such as materials science, agrochemicals, and specialty chemicals. Its unique properties make it a valuable tool for exploring new chemical space and discovering innovative solutions to existing challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 51326-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51326-51:
(7*5)+(6*1)+(5*3)+(4*2)+(3*6)+(2*5)+(1*1)=93
93 % 10 = 3
So 51326-51-3 is a valid CAS Registry Number.
51326-51-3Relevant articles and documents
A mild ligand-free iron-catalyzed liberation of alcohols from allylcarbonates
Dieskau, Andre P.,Plietker, Bernd
supporting information; experimental part, p. 5544 - 5547 (2011/12/05)
Different from most carbonates the allyloxy carbonyl protecting group can be cleaved under neutral conditions using metal catalysis. However, most of the catalysts employed to date are based upon precious metals. Herein we present two protocols for the mild Fe-catalyzed liberation of alcohols from allylcarbonates that are characterized by broad functional group tolerance and exclusive chemoselectivity.
A desilylation and a one-pot desilylation-oxidation of aliphatic tert-butyldimethylsilyl ethers using catalytic quantities of PdCl2(CH3CN)2
Wilson, Noel S.,Keay, Brian A.
, p. 2918 - 2919 (2007/10/03)
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