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2,4-Diethoxybenzoic acid, also known as diethoxybenzoic acid, is a chemical compound characterized by the molecular formula C11H14O4. It is a white solid that exhibits solubility in organic solvents and has a melting point in the range of 95-97°C. 2,4-DIETHOXYBENZOIC ACID is distinguished by its unique chemical structure and properties, which make it a versatile intermediate in various chemical syntheses.

19074-30-7

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19074-30-7 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Diethoxybenzoic acid is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds. Its chemical properties allow it to be a key component in creating a wide array of therapeutic agents.
Used in Fragrance and Flavoring Industry:
2,4-DIETHOXYBENZOIC ACID serves as a building block in the production of fragrances and flavorings, enhancing the sensory qualities of various consumer products. Its ability to be incorporated into complex organic structures makes it valuable in creating distinct scents and tastes.
Used in Organic Electronics and Materials Science:
2,4-Diethoxybenzoic acid has potential applications in the field of organic electronics and materials science. Its unique structure and properties lend themselves to the development of innovative materials with specific electronic characteristics, contributing to advances in technology and material design.

Check Digit Verification of cas no

The CAS Registry Mumber 19074-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19074-30:
(7*1)+(6*9)+(5*0)+(4*7)+(3*4)+(2*3)+(1*0)=107
107 % 10 = 7
So 19074-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-3-14-8-5-6-9(11(12)13)10(7-8)15-4-2/h5-7H,3-4H2,1-2H3,(H,12,13)

19074-30-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Diethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,4-diethoxy-benzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19074-30-7 SDS

19074-30-7Relevant academic research and scientific papers

Rational Design of Rod-Like Liquid Crystals Exhibiting Two Nematic Phases

Mandle, Richard J.,Cowling, Stephen J.,Goodby, John W.

supporting information, p. 14554 - 14562 (2017/10/23)

Recently, a polar, rod-like liquid-crystalline material was reported to exhibit two distinct nematic mesophases (termed N and NX) separated by a weakly first-order transition. Herein, we present our initial studies into the structure–property relationships that underpin the occurrence of the lower-temperature nematic phase, and report several new materials that exhibit this same transformation. We have prepared material with significantly enhanced temperature ranges, allowing us to perform a detailed study of both the upper- and lower-temperature nematic phases by using small-angle X-ray scattering. We observed a continuous change in d spacing rather than a sharp change at the phase transition, a result consistent with a transition between two nematic phases, structures of which are presumably degenerate.

Synthesis and characterization of molecules containing thiazole and oxazole moieties and study of ESIPT phenomenon

Satam, Manjaree A.,Raut, Rajesh K.,Tathe, Abhinav B.,Sekar

, p. 1237 - 1248 (2013/01/15)

Two novel ESIPT molecules, 2-[4-(1,3-benzothiazol-2-yl)naphtho[1,2-d][1,3] oxazol-2-yl]phenol 9a and 4-[4-(1,3-benzothiazol-2-yl)naphtho[1,2-d][1,3]oxazol- 2-yl]benzene-1,3-diol 9b were synthesized by condensing 1-amino-3-(1,3- benzothiazol-2-yl)naphthale

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