24475-36-3

Basic information

• Product Name: 4-(4-tert-butylphenyl)butanoic acid
• Synonyms: 4-(4-tert-butylphenyl)butanoic acid;OTAVA-BB 1043354;UKRORGSYN-BB BBR-020942;4-(4-tert-butylphenyl)butanoic acid(SALTDATA: FREE)
• CAS NO: 24475-36-3
• Molecular Formula: C₁₄H₂₀O₂
• Molecular Weight: 220.31
• Mol File: 24475-36-3.mol
• Article Data: 8

Chemical Properties

• Melting Point: 59.5-60.5 °C
• Boiling Point: 336.6°C at 760 mmHg
• Flash Point: 233.6°C
• Appearance: /
• Density: 1.017g/cm³
• Vapor Pressure: 4.35E-05mmHg at 25°C
• Refractive Index: 1.512
• PKA: 4.77±0.10(Predicted)
• CAS DataBase Reference: 4-(4-tert-butylphenyl)butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-tert-butylphenyl)butanoic acid(24475-36-3)
• EPA Substance Registry System: 4-(4-tert-butylphenyl)butanoic acid(24475-36-3)

Safety Data

• Hazardous Substances Data: 24475-36-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H20O2/c1-14(2,3)12-9-7-11(8-10-12)5-4-6-13(15)16/h7-10H,4-6H2,1-3H3,(H,15,16)

Upstream product

• 996-82-7 sodium diethylmalonate 
• 56829-61-9 1-(2-bromoethyl)-4-(tert-butyl)benzene 
• 108-30-5 succinic acid anhydride 
• 253185-03-4 tert-butylbenzene 
• 35288-08-5 4-(4-tert-butylphenyl)-4-oxobutyric acid 
• 27798-45-4 1-allyl-4-(tert-butyl)benzene 
• 54338-32-8 4-(4-cyclohexylphenyl)butanoic Acid 

Downstream Products

• 18127-01-0 3-(4-tert-butylphenyl)propionaldehyde 
• 78574-08-0 3-(4-tert-butylphenyl)propan-1-ol 
• 127897-29-4 9-[3-(4-tert-Butyl-phenyl)-propyl]-acridine 
• 58567-80-9 1-(tert-butyl)-4-propylbenzene 
• 4838-42-0 9,10,9',10'-tetrahydro-9,9'-biacridyl 
• 124694-03-7 1-(4-bromobutyl)-4-(tert-butyl)benzene 
• 22583-68-2 7-(1,1-dimethylethyl)-3,4-dihydro-1(2H)-naphthalenone 
• 72768-33-3 1-[1,7-bis-(4-t-butylphenyl)-4-heptyl]-1,5,9,13-tetrazatridecane 
• 72781-46-5 1-[1,7-di-(4-t-butylphenyl)-4-heptyl]-1,4,7,10-tetrazadecane 
• 72781-44-3 [3-(3-Amino-propylamino)-propyl]-{4-(4-tert-butyl-phenyl)-1-[3-(4-tert-butyl-phenyl)-propyl]-butyl}-amine 
• 84029-99-2 1,1-Dimethyl-7-t-butylnaphthalene 
• 855220-19-8 4-(4-tert-butyl-phenyl)-butyryl chloride 
• 134030-39-0 ethyl 4-(4-(tert-butyl)phenyl)butanoate 
• 1221819-66-4 4-(4-tert-butylphenyl)-N,N-dimethylbutanamide 

Relevant articles and documents

Carbonylative Transformation of Allylarenes with CO Surrogates: Tunable Synthesis of 4-Arylbutanoic Acids, 2-Arylbutanoic Acids, and 4-Arylbutanals

In this Communication, procedures for the selective synthesis of 4-arylbutanoic acids, 2-arylbutanoic acids, and 4-arylbutanals from the same allylbenzenes have been developed. With formic acid or TFBen as the CO surrogate, reactions proceed selectively and effectively under carbon monoxide gas-free conditions.

SYNTHESIS OF SUBSTITUTED TETRAHYDROINDENYL COMPLEXES

This invention relates to the synthesis of substituted tetrahydroindenyls and the use of the synthesised complexes in the homo- and co-polymerisation of ethylene and alpha-olefins.

AMINO ALCOHOL COMPOUND

A pharmaceutical composition is provided that has a low toxicity, demonstrates superior physicochemical properties and pharmacokinetics, and has superior peripheral blood lymphocyte count lowering activity. The pharmaceutical composition contains a compound having general formula (I): (wherein R 1 represents a methyl group or an ethyl group, R 2 represents a methyl group or an ethyl group, and R 3 represents a phenyl group substituted with 1 to 3 substituents selected from the group consisting of a halogen atom, a lower alkyl group, a cycloalkyl group, a lower alkoxy group, a halogeno lower alkyl group, a lower aliphatic acyl group and a cyano group), a pharmacologically acceptable salt thereof or a pharmacologically acceptable ester thereof.