4653-08-1 Usage
Description
4-OXO-4-(2-THIENYL)BUTYRIC ACID, also known as 4-oxo-4-(2-thienyl)butanoic acid, is a 4-oxo monocarboxylic acid derivative of butyric acid with oxo and 2-thienyl groups at the 4-position. It is characterized by its beige crystalline powder form and exhibits unique chemical properties that make it suitable for various applications across different industries.
Uses
Used in Pharmaceutical Industry:
4-OXO-4-(2-THIENYL)BUTYRIC ACID is used as an intermediate in the synthesis of pharmaceutical compounds for its unique structural features and reactivity. Its presence in the molecular structure can contribute to the development of new drugs with potential therapeutic benefits.
Used in Chemical Synthesis:
In the field of organic chemistry, 4-OXO-4-(2-THIENYL)BUTYRIC ACID is used as a building block for the synthesis of various organic compounds. Its oxo and 2-thienyl groups at the 4-position provide a versatile platform for further chemical reactions and modifications, leading to the creation of novel molecules with specific properties.
Used in Research and Development:
4-OXO-4-(2-THIENYL)BUTYRIC ACID is utilized in research and development settings to explore its potential applications and properties. Scientists and researchers use this compound to investigate its reactivity, stability, and interactions with other molecules, which can lead to the discovery of new applications and insights into its chemical behavior.
Used in Material Science:
In material science, 4-OXO-4-(2-THIENYL)BUTYRIC ACID can be employed as a component in the development of new materials with specific properties. Its unique structure and chemical properties can contribute to the creation of materials with tailored characteristics, such as improved stability, reactivity, or other desirable attributes.
Check Digit Verification of cas no
The CAS Registry Mumber 4653-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4653-08:
(6*4)+(5*6)+(4*5)+(3*3)+(2*0)+(1*8)=91
91 % 10 = 1
So 4653-08-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O3S/c9-6(3-4-8(10)11)7-2-1-5-12-7/h1-2,5H,3-4H2,(H,10,11)/p-1
4653-08-1Relevant articles and documents
NEW SYNTHESIS OF 1-TRIACONTANOL
Bhalerao, U. T.,Rao, Jagadishwar S.,Tilak, B. D.
, p. 5439 - 5440 (1984)
Succinic anhydride and behenic acid have been used to attach C4 and C22 carbon chains on to 2 and 5 positions of thiophene through two alternate acylation sequences.Raney nickel desulphurization to the 2,5-disubstituted thiophene yielded triacontanoic acid esters which on LAH reduction gave 1-triacontanol.
NEAR-INFRARED ABSORBING DYE, OPTICAL FILTER, AND IMAGING DEVICE
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Paragraph 0192; 0194, (2021/03/13)
A near-infrared absorbing dye includes a compound represented by formula (A). Each of R11 to R14 is independently a hydrogen atom, a halogen atom, a hydroxyl group, or an alkyl, aryl or alaryl group. Each of pairs R11 and R12, R12 and R13, and R13 and R14 may combine with one another to form a monocyclic ring or a polycyclic ring in which from 2 to 4 rings are fused. Each of R15 and R16 is independently an alkyl or alaryl group. R15 and R16 may combine with one another to form a cyclohetero ring having from 5 to 10 members together with the nitrogen atom.
Novel synthetic method for duloxetine intermediate
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Paragraph 0008; 0017, (2018/09/08)
The invention provides a novel synthetic method for a duloxetine intermediate (S)-N-methyl-3-hydroxy-3-(2-thienyl)-1-propylamine (a compound 1 as described in the specification). According to the method, thiophene and succinic anhydride are used as raw materials and undergo Friedel-Crafts acylation, esterification, aminolysis, asymmetric hydrogenation, and oxidative degradation so as to obtain theduloxetine intermediate (the compound 1).
