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(2E)-4-[2-Nitro-3-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]phenyl]-4-oxo-2-butenoic Acid Methyl Ester is a complex organic compound characterized by its unique chemical structure. It features a 2-butenoic acid core with a methyl ester group, a phenyl ring substituted with a nitro group and a tetra-O-acetyl-β-D-glucopyranosyloxy group. This molecule is of interest due to its potential applications in various industries.

224044-68-2

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224044-68-2 Usage

Uses

Used in Pharmaceutical Industry:
(2E)-4-[2-Nitro-3-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]phenyl]-4-oxo-2-butenoic Acid Methyl Ester is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Cosmetics Industry:
In the cosmetics industry, (2E)-4-[2-Nitro-3-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]phenyl]-4-oxo-2-butenoic Acid Methyl Ester is used as a key component in the preparation of human UV filters. Its incorporation into sunscreens and other skincare products helps protect the skin from harmful ultraviolet radiation, reducing the risk of sunburn, premature aging, and skin cancer.
Used in Chemical Research:
(2E)-4-[2-Nitro-3-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]phenyl]-4-oxo-2-butenoic Acid Methyl Ester is also utilized in chemical research as a model compound for studying the properties and reactivity of complex organic molecules. This can lead to a better understanding of chemical reactions and the development of new synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 224044-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,0,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 224044-68:
(8*2)+(7*2)+(6*4)+(5*0)+(4*4)+(3*4)+(2*6)+(1*8)=102
102 % 10 = 2
So 224044-68-2 is a valid CAS Registry Number.

224044-68-2Relevant academic research and scientific papers

Synthesis of Human Ultraviolet Filter Compounds: O-β-D-Glucopyranosides of 3-Hydroxykynurenine and 2-Amino-3-hydroxy-γ-oxobenzenebutanoic Acid

Manthey, Michael K.,Jamie, Joanne F.,Truscott, Roger J. W.

, p. 3930 - 3933 (2007/10/03)

The role of endogenous tryptophan-derived UV filters in aging lenses and in human cataract is becoming increasingly important. The two major UV filters found in the lenses of primates, the O-β-D-glucopyranosides of 3-hydroxykynurenine and 2-amino-3-hydroxy-γ-oxobenzenebutanoic acid, 1 and 2, were synthesized from the common benzoyl acrylate precursor 2-amino-3-hydroxybenzoyl-acrylic acid 10. Synthesis of compound 3, the α-N-acetyl derivative of 1, was achieved using coupling of 2-nitro-3-benzyloxyacetophenone 4 with the sodium salt of diethyl acetamidomalonate as a key step. This is the first reported synthesis of the lenticular glucopyranoside 2 and the N-acetyl compound 3.

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