62858-83-7

Basic information

• Product Name: 2-isopropylresorcinol
• Synonyms: 2-isopropylresorcinol;2-(1-Methylethyl)-1,3-benzenediol;2-isopropylbenzene-1,3-diol
• CAS NO: 62858-83-7
• Molecular Formula: C₉H₁₂O₂
• Molecular Weight: 152.19038
• EINECS: 263-743-1
• Mol File: 62858-83-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 293.9°C at 760 mmHg
• Flash Point: 143.6°C
• Appearance: /
• Density: 1.116g/cm³
• Vapor Pressure: 0.000956mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: 2-isopropylresorcinol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-isopropylresorcinol(62858-83-7)
• EPA Substance Registry System: 2-isopropylresorcinol(62858-83-7)

Safety Data

• Hazardous Substances Data: 62858-83-7(Hazardous Substances Data)

Usage

General Description

2-Isopropylresorcinol is a chemical compound that belongs to the resorcinol class of chemicals. It is a derivative of resorcinol and is commonly used in cosmetic and skincare products as a skin-lightening agent. It works by inhibiting the production of melanin in the skin, leading to a brighter and more even complexion. Additionally, 2-Isopropylresorcinol has antioxidant properties which help to protect the skin from damage caused by free radicals. It is considered safe for use in skincare products and has been approved for cosmetic use in various countries.

InChI:InChI=1/C9H12O2/c1-6(2)9-7(10)4-3-5-8(9)11/h3-6,10-11H,1-2H3

Upstream product

• 16700-61-1 1,3-dimethoxy-2-(1-methylethyl)benzene 
• 3401-01-2 2-isopropyl-cyclohexane-1,3-dione 
• 2040-04-2 2,6-dimethoxyacetophenone 
• 25108-61-6 1,3-dimethoxy-2-(1-methylethenyl)benzene 
• 16929-70-7 1,3-dimethoxy-2-(1-hydroxy-1-methylethyl)benzene 

Downstream Products

• 65239-70-5 1-(2,4-Dihydroxy-3-isopropyl-phenyl)-2,2,2-trifluoro-ethanone 
• 139117-27-4 2-isopropyl-4-(4-nitrophenylazo)resorcinol 
• 65240-38-2 1-{5-[2,4-Dihydroxy-3-isopropyl-5-(2,2,2-trifluoro-acetyl)-benzyl]-2,4-dihydroxy-3-isopropyl-phenyl}-2,2,2-trifluoro-ethanone 

Relevant articles and documents

SUBSTITUTED-N-HETEROARYL COMPOUNDS AND USES THEREOF

The present disclosure relates generally to compounds useful for the treatment and/or enhancement of cognitive function and negative symptoms associated with central nervous system disorders where the circuitry involving fast spiking PV+ interneurons and the production of cortical gamma oscillations is disrupted. The subject disclosure enables the manufacture of medicaments as well as compositions containing same for use in methods of therapy and prophylaxis of cognitive dysfunction and negative symptoms.

1 -HYDROXY-BENZOOXABOROLES AS ANTIPARASITIC AGENTS

Provided are compounds useful for controlling endoparasites both in animals and agriculture. Further provided are methods for controlling endoparasite infestations of an animal by administering an effective amount of a compound as described above, or a pharmaceutically acceptable salt thereof, to an animal, as well as formulations for controlling endoparasite infestations using the compounds described above or an acceptable salt thereof, and an acceptable carrier. The claimed compounds are described by the following Markush formula:A typical example for a compound according to above formula is: A typical example for a compound according to above formula is:

Process for the preparation of resorcinol derivatives

2-Substituted-4,6-di-t-butylresorcinol represented by the general formula: STR1 wherein R represents a straight or branched alkyl group having 1 to 20 carbon atoms, a straight or branched alkenyl group having 2 to 20 carbon atoms and at least one double bond, or an aralkyl group, but the tertiary carbon atom of R is free from direct bonding to the benzene nucleus, is prepared by allowing 4,6-di-t-butylresorcinol to react with a halogen compound represented by the general formula: wherein R has the same meaning as defined above, and X represents a halogen atom, excluding the X bonded to the tertiary carbon of R, in an aqueous alkali solution. By further debutylization of the 2-substituted-4,6-t-butylresorcinol, 2-substituted resorcinol represented by the general formula: STR2 wherein R has the same meaning as defined above, but the tertiary carbon of R is free from direct bonding to the benzene nucleus, is prepared.