3062-64-4

Usage

Uses

Used in Organic Synthesis:
3,5-DI-TERT-BUTYL-4-HYDROXYBENZENEPROPANOYL CHLORIDE is used as a reagent in organic synthesis for the preparation of esters and amides. Its reactivity and unique chemical structure make it a valuable component in the synthesis of various organic compounds, contributing to the development of new materials and pharmaceuticals.
Used in Chemical Research:
In the field of chemical research, 3,5-DI-TERT-BUTYL-4-HYDROXYBENZENEPROPANOYL CHLORIDE serves as a key intermediate in the exploration of new chemical reactions and mechanisms. Its properties and reactivity are studied to understand its potential applications and to develop new methods for synthesizing related compounds.
Used in Pharmaceutical Industry:
3,5-DI-TERT-BUTYL-4-HYDROXYBENZENEPROPANOYL CHLORIDE is used as a building block in the pharmaceutical industry for the development of new drugs. Its unique structure and reactivity allow for the creation of novel compounds with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Material Science:
In material science, 3,5-DI-TERT-BUTYL-4-HYDROXYBENZENEPROPANOYL CHLORIDE is utilized in the synthesis of new materials with specific properties. Its role in creating esters and amides can lead to the development of materials with improved characteristics, such as enhanced stability, durability, or specific functional properties, for use in various industries.

InChI:InChI=1/C17H25ClO2/c1-16(2,3)12-9-11(7-8-14(18)19)10-13(15(12)20)17(4,5)6/h9-10,20H,7-8H2,1-6H3

Upstream product

• 95602-92-9 3,5-di-tert-butyl-4-hydroxycinnamic acid 
• 128-39-2 2,6-di-tert-butylphenol 
• 107-13-1 acrylonitrile 

Downstream Products

• 129263-69-0 5,11,17,23-Tetra-tert.-butyl-25,26,27,28-tetrakis-(4'-hydroxy-3,5-di-tert.-butylphenylpropionyl)-calix<4>aren 
• 34249-71-3 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamide 
• 80829-22-7 2,2-Dimethyl-3-stearamidopropyl 3-(3,5-di-tert-butyl-4-hydroxylphenyl)propionate 
• 52449-47-5 4-[3-(3,5-di-tert-butyl-4-hydroxy-phenyl)-propionyl]-morpholine 
• 52449-48-6 N-benzyl-3-(3,5-di-tert-butyl-4-hydroxy)phenylpropanamide 
• 24413-56-7 1,3,5-tris-[3-(3,5-Di-t-butyl-4-hydroxyphenyl)-propionyloxy]-2,2,4,4,6,6-hexamethylcyclohexane 
• 185053-75-2 Co(C₃₂H₁₂N₈)(C₁₇H₂₆NO₂)4 

Relevant academic research and scientific papers

N-(carbonyl, carbonimidoyl, carbonothioyl)sulfonamide charge control agents and toners and developers

An electrophotographic toner having polymeric binder and a charge control agent selected from the group consisting of sulfonamides having the general structure: STR1 and metal salts thereof. T1 is independently selected from H, alkyl having from 1 to 20 carbons, cycloalkyl having from 3 to 18 carbons, and aromatic and heteroaromatic ring systems having a solitary ring or 2 to 3 linked or fused rings. R1 is O, S, N--H, N--R5, or N--L--R5 ; where L is a linking group selected from: STR2 and R5 is independently selected from alkyl having from 1 to 20 carbons, cycloalkyl having from 3 to 18 carbons, and aromatic and heteroaromatic ring systems having a solitary ring or 2 to 3 linked or fused rings. L1 and L2 are each independently a direct link or divalent alkyl or fluoroalkyl having from 1 to 20 carbons. Ra and Rb are each independently selected from the group consisting of H, F and ring systems having a solitary ring or from 2 to 3 fused or linked rings, said ring system having from 3 to 34 carbons, including carbons of substituent groups. If L1 is a direct link, Ra is a ring system and if L2 is a direct link, Rb is a ring system.