189256-18-6 Usage
Uses
Used in Food Industry:
Benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is used as a food preservative for its antimicrobial properties, which help to extend the shelf life of food products and prevent spoilage.
Used in Pharmaceutical Industry:
Benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is used as an intermediate in the synthesis of various chemicals, contributing to the development of new drugs and treatments.
Used in Plastics Industry:
Benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is used in the production of plastics, where its properties can enhance the performance and stability of the final product.
Used in Perfumery and Cosmetics Industry:
Benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is used in the production of perfumes and dyes, where its aromatic properties contribute to the creation of various fragrances and colorants.
Used in Chemical Synthesis:
As an intermediate in chemical synthesis, benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is utilized in the development of a wide range of chemical products, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Drug Development:
Due to its potential applications in the development of new drugs and treatments, benzoic acid, 2-[[(1,4-dioxopentyl)oxy]methyl]is an important compound in the field of drug discovery and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 189256-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,2,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 189256-18:
(8*1)+(7*8)+(6*9)+(5*2)+(4*5)+(3*6)+(2*1)+(1*8)=176
176 % 10 = 6
So 189256-18-6 is a valid CAS Registry Number.
189256-18-6Relevant academic research and scientific papers
Kamaike, Kazuo,Takahashi, Hiroaki,Kakinuma, Takashi,Morohoshi, Kimio,Ishido, Yoshiharu
, p. 6857 - 6860 (1997)
A novel 2-(levulinyloxymethyl)-5-nitrobenzoyl (LMNBz) protecting group for the 5' position of nucleoside 3'-phosphoramidites was successfully applied to the solid-phase synthesis of both an oligodeoxyribonucleotide (TpTpT and TpTpTpT) and an octaribonucleotide in combination with a 2'-O-Thp protecting group (UpCpApGpUpUpGpG). The LMNBz group was simply unmasked due to its base-labile property by a two-step procedure, i.e., treatments with 0.5 M hydrazine hydrate in 1:4 acetic acid - pyridine, and then with 0.5 M imidazole in acetonitrile.