18167-33-4

Basic information

• Product Name: METHYL 2-N-PROPYLOXYBENZOATE
• Synonyms: METHYL 2-N-PROPYLOXYBENZOATE;Methyl 2-n-propyloxybenzoate 90%+;Benzoic acid, 2-propoxy-, methyl ester
• CAS NO: 18167-33-4
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Product Categories: Anisoles, Alkyloxy Compounds & Phenylacetates;Acids & Esters
• Mol File: 18167-33-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 275.531°C at 760 mmHg
• Flash Point: 110.331°C
• Appearance: /
• Density: 1.054g/cm³
• Vapor Pressure: 0.005mmHg at 25°C
• Refractive Index: 1.497
• CAS DataBase Reference: METHYL 2-N-PROPYLOXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-N-PROPYLOXYBENZOATE(18167-33-4)
• EPA Substance Registry System: METHYL 2-N-PROPYLOXYBENZOATE(18167-33-4)

Safety Data

• Hazardous Substances Data: 18167-33-4(Hazardous Substances Data)

Usage

Description

METHYL 2-N-PROPYLOXYBENZOATE is an organic compound that serves as a fragrance ingredient in a variety of products. It is characterized by its clear, colorless liquid form and a sweet, floral scent. This chemical is predominantly utilized as a fixative to enhance the stability and longevity of the aroma in numerous products, while also contributing to skin-conditioning properties in skincare and haircare formulations.

Uses

Used in Cosmetics and Personal Care Products:
METHYL 2-N-PROPYLOXYBENZOATE is used as a fragrance ingredient for its sweet, floral odor, adding pleasant scents to cosmetics and personal care products.
Used in Household Goods:
METHYL 2-N-PROPYLOXYBENZOATE is used as a fragrance ingredient in household goods to provide a fresh and appealing scent, enhancing the overall sensory experience of using these products.
Used as a Fixative:
METHYL 2-N-PROPYLOXYBENZOATE is used as a fixative to help stabilize and prolong the aroma of other volatile compounds in various products, ensuring a consistent and lasting fragrance.
Used in Skincare Formulations:
METHYL 2-N-PROPYLOXYBENZOATE is used as a skin-conditioning agent in skincare products, contributing to the health and appearance of the skin.
Used in Haircare Formulations:
METHYL 2-N-PROPYLOXYBENZOATE is used as a skin-conditioning agent in haircare products, promoting healthier and better-maintained hair.

InChI:InChI=1/C11H14O3/c1-3-8-14-10-7-5-4-6-9(10)11(12)13-2/h4-7H,3,8H2,1-2H3

Upstream product

• 107-08-4 1-iodo-propane 
• 119-36-8 methyl salicylate 
• 26930-28-9 2-(3-bromo-propoxy)-benzoic acid methyl ester 
• 106-94-5 propyl bromide 
• 682-01-9 tetrapropoxysilane 
• 610-97-9 o-iodo-methyl-benzoic acid 
• 75-91-2 tert.-butylhydroperoxide 
• 2100-31-4 2-propoxybenzoic acid 

Downstream Products

• 2100-31-4 2-propoxybenzoic acid 
• 108463-11-2 1-(2-Propoxyphenyl)-3-(1,2,3,4-tetrahydro-1-oxo-2-naphthalenyl)-1,3-propanedione 
• 252233-56-0 methyl 5-chlorosulfonyl-2-propoxybenzoic acid 
• 252233-62-8 (R)-5-[(3-(dimethylamino)pyrrolidinyl)sulfonyl]-2-propoxybenzoic acid 
• 321307-30-6 (S)-5-[(3-(dimethylamino)pyrrolidinyl)sulfonyl]-2-propoxybenzoic acid 
• 252233-59-3 5-((R)-3-Dimethylamino-pyrrolidine-1-sulfonyl)-2-propoxy-benzoic acid methyl ester 
• 215299-79-9 5-(4-Ethylpiperazin-1-ylsulphonyl)-2-n-propoxybenzoic Acid 
• 252233-58-2 5-(4-ethyl-piperazine-1-sulfonyl)-2-propoxy-benzoic acid methyl ester 
• 1026085-98-2 5-(4-ethyl-piperazine-1-sulfonyl)-2-propoxy-benzoyl chloride 

Relevant articles and documents

Copper-catalyzed oxidative methyl-esterification of 5-hydroxymethylfurfural using TBHP as an oxidizing and methylating reagent: A new approach for the synthesis of furan-2,5-dimethylcarboxylate

Catalytic conversion of 5-hydroxymethylfurfural (HMF) into furan-2,5-dimethylcarboxylate (FDMC) is of great significance in the production of polyethylene furanoate (PEF), a renewable biomass-derived polymer that can replace the fossil dependent polyethylene terephthalate (PET). Herein, for the first time, we report the synthesis of FDMC from oxidative methyl-esterification of HMF using tert-butyl hydroperoxide (TBHP) as an oxidizing and methylating reagent catalyzed by mesoporous alumina nanospheres-embedded with CuO nanoparticles (CuO/m-Al2O3). The CuO/m-Al2O3 catalysts with different copper contents were prepared by evaporation-induced self-assembly of a structure-directing agent (Pluronic P-123). The decomposition of P-123 during calcination in air results into the formation of a mesoporous structure with highly dispersed CuO nanoparticles. The as-prepared 6-CuO/m-Al2O3 exhibits excellent catalytic activity towards oxidative methyl-esterification of HMF into FDMC with 92% yield and turnover frequency (TOF) of 0.56 h?1. Furthermore, oxidative methyl-esterification of a range of substrates through SP3 C[sbnd]H bond functionalization has also been demonstrated using the same catalyst.

SULPHAMOYLARYL DERIVATIVES AND USE THEREOF AS MEDICAMENTS FOR THE TREATMENT OF LIVER FIBROSIS

Potent 5-HT2B antagonist of Formula (A), including stereochemically isomeric forms, and salts, hydrates, solvates thereof and their use wherein R1 to R4 and Ar have the meaning as defined herein. The present invention also relates to processes for preparing said compounds, pharmaceutical compositions containing them, alone or in combination with other drugs, in fibrosis and/or cirrhosis prevention or therapy.

Optimization of substituted N-3-benzylimidazoquinazolinone sulfonamides as potent and selective PDE5 inhibitors

A previous report from these laboratories identified the N-3-benzylimidazoquinazolinone nucleus as a more selective PDE5 inhibitor template compared to the pyrazolopyrimidine of sildenafil. This paper describes in detail the structure-activity relationshi