2,6-Dichlorophenylacetic acid

2,6-Dichlorophenylacetic acid
  • CAS No.:6575-24-2
Other grades of this product :
2,6-Dichlorophenylacetic acid Basic information
Uses
Product Name:2,6-Dichlorophenylacetic acid
Synonyms:2-(2,6-DICHLOROPHENYL)ACETIC ACID;2,6-DICHLORO BENZENEACETIC ACID;2,6-DICHLOROPHENYLACETIC ACID;RARECHEM AL BO 0115;TIMTEC-BB SBB003503;2,6-Dichlorphenylessigsure;Guanfacine Impurity 1;Benzeneacetic acid, 2,6-dichloro-
CAS:6575-24-2
MF:C8H6Cl2O2
MW:205.04
EINECS:229-504-0
Product Categories:C8;Carbonyl Compounds;Acids and Derivatives;Aromatic Phenylacetic Acids and Derivatives;Phenylacetic acid;Carboxylic Acids
Mol File:6575-24-2.mol
2,6-Dichlorophenylacetic acid Chemical Properties
Melting point 158-161 °C (lit.)
Boiling point 294.45°C (rough estimate)
density 1.3806 (rough estimate)
refractive index 1.5490 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka3.80±0.10(Predicted)
color White to Off-White
BRN 1952744
CAS DataBase Reference6575-24-2(CAS DataBase Reference)
NIST Chemistry Reference2,6-Dichlorophenylacetic acid(6575-24-2)
EPA Substance Registry SystemBenzeneacetic acid, 2,6-dichloro- (6575-24-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26-26/37/39-36
WGK Germany 3
Hazard Note Irritant
HS Code 29163900
MSDS Information
ProviderLanguage
2,6-Dichlorophenylacetic acid English
ACROS English
ALFA English
2,6-Dichlorophenylacetic acid Usage And Synthesis
Uses2,6-Dichlorophenylacetic acid is an inhibitor of isopenicillin N synthase (IPNS) and acyl-CoA: 6-APA acyltransferase. 2,6-Dichlorophenylacetic acid is also part of a group of phenylacetate derivatives that have cytostatic activity against tumour cells.
Chemical Propertieswhite crystalline powder
Uses2,6-Dichlorophenylacetic acid is an inhibitor of isopenicillin N synthase (IPNS) and acyl-CoA: 6-APA acyltransferase. 2,6-Dichlorophenylacetic acid is also part of a group of phenylacetate derivatives that have cytostatic activity against tumour cells.
Purification MethodsCrystallise the acid from aqueous EtOH. [Beilstein 9 III 2272.]

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