17302-82-8

Basic information

• Product Name: ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE
• Synonyms: RARECHEM AL BI 0933;3,5-DICHLORO-4-HYDROXYBENZOIC ACID ETHYL ESTER;LABOTEST-BB LT00455658;ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE;3,5-dichloro-4-hydroxy-benzoicaciethylester;ethyl3,5-dlchloro-4-hydroxybenzoate;Benzoic acid, 3,5-dichloro-4-hydroxy-, ethyl ester;Ethyl=4-hydroxy-3,5-dichlorobenzoate
• CAS NO: 17302-82-8
• Molecular Formula: C₉H₈Cl₂O₃
• Molecular Weight: 235.06
• EINECS: 241-331-2
• Product Categories: Aromatic Esters;Phenyls & Phenyl-Het;Esters;Phenyls & Phenyl-Het
• Mol File: 17302-82-8.mol

Chemical Properties

• Melting Point: 98-102 °C
• Boiling Point: 335.78°C (rough estimate)
• Flash Point: 145.3 °C
• Appearance: beige powder
• Density: 1.3965 (rough estimate)
• Vapor Pressure: 0.000219mmHg at 25°C
• Refractive Index: 1.5000 (estimate)
• Storage Temp.: Refrigerator
• Solubility: Soluble in methanol.
• BRN: 2649965
• CAS DataBase Reference: ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE(17302-82-8)
• EPA Substance Registry System: ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE(17302-82-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 24/25
• RTECS: DG7503500
• Hazardous Substances Data: 17302-82-8(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE is used as a key intermediate for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pharmaceutical Industry:
ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE is used as a building block in the development of pharmaceutical products, playing a significant role in the creation of new drugs and medications.
Used in Agrochemical Industry:
ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE is used as an intermediate in the production of agrochemicals, such as pesticides and herbicides, to help protect crops and enhance agricultural productivity.
Used in Dyestuff Industry:
ETHYL 3,5-DICHLORO-4-HYDROXYBENZOATE is used as a starting material in the synthesis of dyes and pigments, contributing to the development of a wide range of colorants for various applications, including textiles, plastics, and inks.

InChI:InChI=1/C9H8Cl2O3/c1-2-14-9(13)5-3-6(10)8(12)7(11)4-5/h3-4,12H,2H2,1H3

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 64-17-5 ethanol 
• 3336-41-2 3,5-dichloro-4-hydroxybenzoic acid 

Downstream Products

• 107418-89-3 3,5-dichloro-4-(2-hydroxy-3-piperidino-propoxy)-benzoic acid ethyl ester 
• 24295-27-0 methyl 3,5-dichloro-4-methoxybenzoate 
• 3336-41-2 3,5-dichloro-4-hydroxybenzoic acid 
• 857537-88-3 4-acetoxy-3,5-dichloro-benzoic acid ethyl ester 
• 38524-86-6 3,5-Dichloro-4-(ethoxy-propylsulfanyl-phosphoryloxy)-benzoic acid ethyl ester 
• 386213-24-7 4-(2-bromo-ethoxy)-3,5-dichloro-benzoic acid ethyl ester 
• 5348-07-2 2-chloro-6-(prop-2-en-1-yl)phenol 
• 87-65-0 2,6-Dichlorophenol 
• 6267-90-9 1,3-dichloro-2-(2-propenyloxy)benzene 
• 73255-04-6 4-allyl-2,6-dichloro-phenol 
• 129527-09-9 1-(3,5-dichloro-4-hydroxy-phenyl)-butan-1-one 
• 129527-08-8 butyric acid-(2,6-dichloro-phenyl ester) 
• 367953-28-4 3,5-dichloro-4-(3-isopropyl-4-methoxy-phenoxy)-benzoic acid ethyl ester 
• 367953-33-1 3,5-dichloro-4-(4-methoxy-phenoxy)-benzoic acid ethyl ester 

Relevant articles and documents

Synthesis method of photosensitive material stabilizing agent of 4-hexadecyloxy carbonyloxy-3,5-dichlorobenzene ethyl formate

The invention relates to a novel synthesis method of a photosensitive material stabilizing agent of 4-hexadecyloxy carbonyloxy-3,5-dichlorobenzene ethyl formate. 4-hydroxyl-3,5-dichlorobenzene ethyl formate is used as raw materials to take a reaction with hexadecyloxy carbonyl acyl chloride under the effect of acid-binding agents to obtain the 4-hexadecyloxy carbonyloxy-3,5-dichlorobenzene ethyl formate. The invention relates to a synthesis method of intermediates of 4-hydroxy-3,5-dichlorobenzene ethyl formate and the hexadecyloxy carbonyl acyl chloride, and the optimum reaction condition of the synthesis of the 4-hexadecyloxy carbonyloxy-3,5-dichlorobenzene ethyl formate, and provides a novel economical and practical method realizing simple operation.

Isomorphous crystals by chloro-methyl exchange in polymorphic fuchsones

The X-ray crystal structures of four fuchsone derivatives in which a chloro group is replaced by methyl were analyzed to understand isostructurality upon Cl-Me exchange in a polymorphic family of molecules. The four methyl groups in tetramethyl fuchsone (TMF, 2,6-dimethyl and α,α-di-p-tolyl) were substituted with chlorine pairwise to give dichloro dimethyl (CMF, 2,6-dichloro and α,α-di-p-tolyl), dimethyl dichloro (MCF, 2,6-dimethyl and α,α-di-p-chlorophenyl), and tetrachloro derivatives (TCF, 2,6-dichloro and α,α-di-p-chlorophenyl). The first three compounds are polymorphic, whereas TCF afforded one crystal modification only. TMF, CMF, and MCF are isostructural and isomorphous crystals in the category of polymorphs, solid solutions, and solvates. The first case of color polymorphism in fuchsone dyes is reported for CMF dimorphs. The formation of solid solution is one of the most stringent tests of isostructutality, which was observed for TMF, CMF, and MCF but not for TCF. Crystal packing in TCF is dominated by short Cl·Cl interactions, and consequently this crystal structure is different from the first three members which are largely a result of space filling. Crystal structures were analyzed using the XPac program to calculate the dissimilarity index of supramolecular constructs and Hirshfeld fingerprint plots to quantify the contribution of Cl·Cl interactions. Isostructurality was observed up to 50% exchange of Cl with Me, but after that point the structure deviates to another packing motif.