19728-20-2

Basic information

• Product Name: (5-ISOPROPYL-2-METHYLPHENOXY)ACETIC ACID
• Synonyms: (5-isopropyl-2-methylphenoxy)acetic acid; [2-methyl-5-(propan-2-yl)phenoxy]acetic acid; [2-methyl-5-(1-methylethyl)phenoxy]acetate
• CAS NO: 19728-20-2
• Molecular Formula: C₁₂H₁₆O₃
• Molecular Weight: 208.26
• Mol File: 19728-20-2.mol
• Article Data: 8

Chemical Properties

• Melting Point: 190-191.5 °C
• Boiling Point: 322.6°C at 760 mmHg
• Flash Point: 119.5°C
• Appearance: /
• Density: 1.090±0.06 g/cm3(Predicted)
• Vapor Pressure: 0.000114mmHg at 25°C
• PKA: 3.24±0.10(Predicted)
• CAS DataBase Reference: (5-ISOPROPYL-2-METHYLPHENOXY)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (5-ISOPROPYL-2-METHYLPHENOXY)ACETIC ACID(19728-20-2)
• EPA Substance Registry System: (5-ISOPROPYL-2-METHYLPHENOXY)ACETIC ACID(19728-20-2)

Safety Data

• Hazardous Substances Data: 19728-20-2(Hazardous Substances Data)

Usage

General Description

(5-Isopropyl-2-methylphenoxy)acetic acid is a chemical compound that belongs to the family of acetic acids and phenols. It is also known by its chemical name, 2-Methyl-4-(1-methylethyl)phenoxyacetic acid. (5-ISOPROPYL-2-METHYLPHENOXY)ACETIC ACID is commonly used as a herbicide in agriculture to control broadleaf weeds and woody plants. It works by disrupting the growth and development of the targeted plants. (5-Isopropyl-2-methylphenoxy)acetic acid is also used in research and as a raw material in the synthesis of other organic compounds. It is important to handle this chemical with care and follow safety guidelines, as it can be harmful if ingested, inhaled, or comes into contact with the skin.

InChI:InChI=1/C12H16O3/c1-8(2)10-5-4-9(3)11(6-10)15-7-12(13)14/h4-6,8H,7H2,1-3H3,(H,13,14)/p-1

Upstream product

• 499-75-2 carvacrol 
• 79-11-8 chloroacetic acid 
• 105-39-5 chloroacetic acid ethyl ester 

Downstream Products

• 20154-41-0 4-isopropyl-2-hydroxybenzoic acid 
• 95725-65-8 2-(5-isopropyl-2-methylphenoxy)acetylchloride 
• 97282-05-8 <2-Methyl-5-isopropyl-phenoxy>-essigsaeure- 
• 97804-98-3 <2-Methyl-5-isopropyl-phenoxy>-essigsaeure- 

Relevant articles and documents

Synthesis, anticholinesterase activity and molecular modeling studies of novel carvacrol-substituted amide derivatives

In the present study, 23 novel carvacrol derivatives involving the amide moiety as a linker between the alkyl chains and/or the heterocycle nucleus were synthesized and tested in vitro as acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) inhib

Betulin-derived compounds as inhibitors of alphavirus replication

This paper describes inhibition of Semliki Forest virus (SFV) replication by synthetic derivatives of naturally occurring triterpenoid betulin (1). Chemical modifications were made to OH groups at C-3 and C-28 and to the C-20-C-29 double bond. A set of heterocyclic betulin derivatives was also assayed. A free or acetylated OH group at C-3 was identified as an important structural contributor for anti-SFV activity, 3,28-di-O-acetylbetulin (4) being the most potent derivative (IC50 value 9.1 μM). Betulinic acid (13), 28-O-tetrahydropyranylbetulin (17), and a triazolidine derivative (41) were also shown to inhibit Sindbis virus, with IC50 values of 0.5, 1.9, and 6.1 μM, respectively. The latter three compounds also had significant synergistic effects against SFV when combined with 3′-amino-3′-deoxyadenosine. In contrast to previous work on other viruses, the antiviral activity of 13 was mapped to take place in virus replication phase. The efficacy was also shown to be independent of external guanosine supplementation.

BETULIN DERIVED COMPOUNDS USEFUL AS ANTIBACTERIAL AGENTS

The invention relates to compouns derived from betulin, and to the use thereof as antibacterial agents in pharmaceutical and cosmetic applications.