152375-23-0 Usage
Description
(2R,3R)-3-[(1R)-1-hydroxyhexyl]oxirane-2-carbaldehyde, also known as oxirane-2-carbaldehyde, is a chiral compound with a complex structure that features an oxirane ring, a hydroxyhexyl side chain, and a carbaldehyde functional group. This versatile chemical serves as a crucial building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, as well as an intermediate in organic synthesis for the production of natural products and functionalized materials.
Uses
Used in Pharmaceutical Synthesis:
(2R,3R)-3-[(1R)-1-hydroxyhexyl]oxirane-2-carbaldehyde is used as a key intermediate for the development of pharmaceuticals, leveraging its unique structural features to create new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, (2R,3R)-3-[(1R)-1-hydroxyhexyl]oxirane-2-carbaldehyde is utilized as a building block for the synthesis of novel agrochemicals, contributing to the development of more effective and environmentally friendly products.
Used in Organic Synthesis:
(2R,3R)-3-[(1R)-1-hydroxyhexyl]oxirane-2-carbaldehyde is employed as an intermediate in organic synthesis, particularly for the production of natural products and functionalized materials, due to its complex and reactive structure.
Used in Material Science:
(2R,3R)-3-[(1R)-1-hydroxyhexyl]oxirane-2-carbaldehyde has potential applications in the development of new materials, such as polymers and catalysts, where its unique structural features can be harnessed to create innovative and high-performance materials.
Check Digit Verification of cas no
The CAS Registry Mumber 152375-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,3,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152375-23:
(8*1)+(7*5)+(6*2)+(5*3)+(4*7)+(3*5)+(2*2)+(1*3)=120
120 % 10 = 0
So 152375-23-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c1-2-3-4-5-7(11)9-8(6-10)12-9/h6-9,11H,2-5H2,1H3/t7-,8+,9-/m1/s1
152375-23-0Relevant articles and documents
Synthesis of the four stereoisomers of 2,3-epoxy-4-hydroxynonanal and their reactivity with deoxyguanosine
Petrova, Katya V.,Stec, Donald F.,Voehler, Markus,Rizzo, Carmelo J.
experimental part, p. 1960 - 1971 (2011/04/22)
2,3-Epoxy-4-hydroxynonanal (EHN) is a potential product of lipid peroxidation that gives rise to genotoxic etheno adducts. We have synthesized all four stereoisomers of EHN and individually reacted them with 2′-deoxyguanosine. In addition to 1,N2-etheno-2′- deoxyguanosine, 12 stereoisomeric products were isolated and characterized by 1H NMR and circular dichroism spectroscopy. The stereochemical assignments were consistent with selective NOE spectra, vicinal coupling constants, and molecular mechanics calculations. Reversed-phase HPLC conditions were developed that could separate most of the adduct mixture.
