5432-17-7

Basic information

• Product Name: ETHYL M-ETHOXYBENZOATE
• Synonyms: ETHYL-3-ETHOXYBENZOATE;ETHYL M-ETHOXYBENZOATE;RARECHEM AL BI 0250;Nsc7016
• CAS NO: 5432-17-7
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Product Categories: C10 to C11;Carbonyl Compounds;Esters
• Mol File: 5432-17-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 152 °C35 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.06 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00996mmHg at 25°C
• Refractive Index: n20/D 1.508(lit.)
• CAS DataBase Reference: ETHYL M-ETHOXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL M-ETHOXYBENZOATE(5432-17-7)
• EPA Substance Registry System: ETHYL M-ETHOXYBENZOATE(5432-17-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 23-26-36
• WGK Germany: 3
• Hazardous Substances Data: 5432-17-7(Hazardous Substances Data)

Usage

General Description

Ethyl m-ethoxybenzoate, also known as ethyl 3-methoxybenzoate, is an organic compound commonly used as a fragrance ingredient in various personal care and cosmetic products. It is a clear liquid with a sweet, floral, and slightly fruity odor. This chemical is derived from benzoic acid and ethyl alcohol and is often added to perfumes, lotions, soaps, and other scented products to impart a pleasant aroma. It is known for its ability to enhance and prolong the fragrance of a product, making it a popular choice for use in the formulation of perfumes and other scented items. However, it is important to note that ethyl m-ethoxybenzoate may cause skin irritation in some individuals and should be used with caution.

InChI:InChI=1/C11H14O3/c1-3-13-10-7-5-6-9(8-10)11(12)14-4-2/h5-8H,3-4H2,1-2H3

Upstream product

• 74-96-4 ethyl bromide 
• 7781-98-8 ethyl-3-hydroxybenzoate 
• 75-03-6 ethyl iodide 
• 99-06-9 3-Carboxyphenol 
• 109-63-7 boron trifluoride diethyl etherate 
• 64-17-5 ethanol 
• 24398-88-7 ethyl 3-bromobenzoate 

Downstream Products

• 928264-55-5 3-(3-ethoxyphenyl)-3-oxopropanenitrile 
• 27830-16-6 3-ethoxybenzoylhydrazide 
• 1053266-43-5 N-[(2R,3R,3aS,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yl]-3-ethoxy-benzamide 
• 33696-05-8 ethyl 3-(benzoyloxy)benzoate 
• 621-51-2 3-ethoxybenzoic acid 
• 110248-48-1 (3-ethoxy-phenyl)-diphenyl-methanol 

Relevant articles and documents

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Oxalic Diamides and tert-Butoxide: Two Types of Ligands Enabling Practical Access to Alkyl Aryl Ethers via Cu-Catalyzed Coupling Reaction

A robust and practical protocol for preparing alkyl aryl ethers has been developed, which relies on using two types of ligands to promote Cu-catalyzed alkoxylation of (hetero)aryl halides. The reaction scope is very general for a variety of coupling partners, particularly for challenging secondary alcohols and (hetero)aryl chlorides. In case of coupling with aryl chlorides and bromides, two oxalic diamides serve as the powerful ligands. The tert-butoxide is first demonstrated as a ligand for Cu-catalyzed coupling reaction, leading to alkoxylation of aryl iodides complete at room temperature. Additionally, a number of carbohydrate derivatives are applicable for this coupling reaction, affording the corresponding carbohydrate-aryl ethers in 29-98% yields.

Composition FOR PREVENTING ALOPECIA AND ACTIVATING HAIR GROWTH

The present invention provides a hair growth promoter comprising as an active ingredient, a compound having a chemical structure of general formula (1) or a pharmacologically acceptable salt thereof. In the general formula (1): R_1 is a saturated or unsaturated straight chain or branched C1-C10 alkyl group or hydroxy alkyl group; R_2 is hydrogen or a saturated or unsaturated straight chain or branched C1-C10 alkoxy or hydroxy alkoxy; X is hydrogen, hydroxy, or a saturated or unsaturated straight chain or branched C1-C10 alkyl group, alkoxy or hydroxyl alkoxy; R_3 and R_4 are each independently selected from R_5, hydrogen, aldehyde, and a saturated or unsaturated straight chain or branched alkyl, alkoxy, or hydroxy alkoxy; R_5 has a structure of # AAA #; R_6 is selected from hydrogen, and a saturated or unsaturated straight chain or branched C1-C10 alkyl, alkoxy, or hydroxy alkoxy; and one of R_3 and R_4 is hydrogen.COPYRIGHT KIPO 2017