2,4,5-Trifluorophenylacetic acid

HCID 2777950CAS 209995-38-0

Grundinformationen

Standard-SMILES
O=C(O)Cc1cc(F)c(F)cc1F
InChIKey
YSQLGGQUQDTBSL-UHFFFAOYSA-N
Summenformel
C8H5F3O2
Durchschnittliche Molmasse
190,12 g/mol
Monoisotopische Masse
190,02416406

Namen und Bezeichner

Bevorzugter Name
2,4,5-Trifluorophenylacetic acid
IUPAC
2-(2,4,5-trifluorophenyl)acetic acid
Englischer Name
2,4,5-Trifluorophenylacetic acid
Summenformel
C8H5F3O2
Molmasse
190.12

Namen und Synonyme

2,4,5-Trifluorophenylacetic acid2-(2,4,5-trifluorophenyl)acetic Acid(2,4,5-trifluorophenyl)acetic acidDTXSID50380723RefChem:442784DTXCID80331748466-070-3606-684-2209995-38-0Benzeneacetic acid, 2,4,5-trifluoro-2,4,5-Trifluorobenzeneacetic AcidMFCD00082479
Weitere Namen anzeigen
2,4,5-Trifluoropheny2,4,5-Trifluorophenylacetic acid ,99%RETAG-001RARECHEM AL BO 05102,4,5-Trifluoropheny245Trifluorophenylacetic Acitrifluorophenylacetic acid5-Trifluorophenylacetic acid2,4,5-trifluoropheylacetic acid2,4,5-trfluorophenylacetic acid
2,4,5-Trifluorophenylaceticacid2,4,5-Trifiuorophenylacetic acid2,4,5-trifluorophenyl acetic acid2-NITRO-P-TOLYLDISULFIDESitagliptin impurity RSCHEMBL332576(2,4,5-trifluorophenyl)-acetic acidT2407

Datenbank-Bezeichner

CAS
209995-38-0
PubChem CID
2777950
DTXSID
DTXSID50380723
UNII
5J2RZ88UH7
EC Number
466-070-3、606-684-2
Nikkaji
J2.103.145C

Eigenschaften

Berechnete Struktureigenschaften

XLogP
1,7
Polarare Oberfläche (TPSA)
37,3 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
5
Frei drehbare Bindungen
2
Schwere Atome
13

Physikochemische Eigenschaften

Schmelzpunkt
121 · 121-125 °C
Siedepunkt
255 · 255.0±35.0 °C(Predicted)
Dichte
1.468 · 1.468±0.06 g/cm3(Predicted)
storage temp.
Sealed in dry,Room Temperature
Löslichkeit
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
Aggregatzustand
Solid

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H315 (98%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 50 reports by companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

This chemical does not meet GHS hazard criteria for 20% (2 of 10) of reports.

Warning

Gefahrenhinweise

Regulatory Information · 2 Einträge

REACH registered substance: 2-(2,4,5-trifluorophenyl)acetic acid (EC: 466-070-3)

REACH registered substance: 2,4,5-Trifluorophenylacetic acid (EC: 606-684-2)

Hazard Classes and Categories · 2 Einträge

Skin Irrit. 2 (98%)

Acute Tox. 4 (60%)

Sicherheitsdaten

wgk
3
hs_code
29163990
risk_code
37/38-41
hazard_code
Xi
safety_code
26-39
hazard_class
IRRITANT

Chemie und Industrie

Anwendungen · 2 Einträge

Beschreibung2,4,5-Trifluorophenylacetic acid is a fluorophenylacetic acid, which is a valuable intermediate for preparing various pharmacologically active compounds. In particular, trifluorophenylacetic acids are used to prepare inhibitors of the dipeptidyl peptidase-4 enzyme. These medicines are helpful in treating diabetes, in particular type 2 diabetes. One of these active ingredients is Sitagliptin, available commercially under the brand name Januvia, which uses 2,4,5-trifluorophenylacetic acid as a critical intermediate for its synthesis.

Verwenden2,4,5-Trifluorobenzeneacetic Acid is used in the synthesis of EGFR/ErbB-2-kinase inhibitors. Also used in the synthesis of new imidazopyrazinone derivatives as potnetial dipeptidyl peptidase IV inhibitors.

Darstellung · 1 Eintrag

synthetischesynthesis of 2,4,5-trifluorophenylacetic acid: A 100 mL flask was charged 10.0 g of 2,4,5-trifluoromandelic acid, 23.9 g of H3PO3 (6 eq.), 0.73 g of Nal (0.1 eq.) and 0.47 g (0.10 eq.) of MSA. The obtained mixture was stirred at 95-105°C for 24 hrs. Once the conversion is completed (by HPLC; conversion > 99%, typically achieved after 24 hours), the mixture is cooled to room temperature, and 20 mL of methyl tert-butyl ether were added and then 20 mL of water where added. The obtained mixture was stirred for 5 min, then the organic layers were separated. Then 10 mL of methyl tert-butyl ether was added to the aqueous layers, stirred for 5 min, then the phase were separated. The organic layers were combined. The combined organic layers were concentrated under vacuum at 35°C, to provide crude 2,4,5-trifluorophenylacetic acid(TFPAA). To the obtained crude TFPAA was recrystallized from toluene, to obtain TFPAA, as a white crystals, 6.4 g, molar yield 69.5%, chemical purity of HPLC 99.47% A/A%

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