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HCID 21784096Erstellt: 27. Oktober 2026

2-Bromo-5-methoxybenzonitrile

KML-45 · 4-Bromo-3-cyanoanisole · 2-BROMO-5-METHOXYBENZONITRILE · Benzonitrile, 2-bromo-5-methoxy- · 2-BroMo-5-Methoxybenzonitrile 97% · 4-Bromo-3-cyanoanisole, 6-Bromo-m-anisonitrile

https://huagongshe.com/de/chemical/21784096

Molekülstruktur von 2-Bromo-5-methoxybenzonitrile

Identifikatoren & physikalische Daten

CAS No.138642-47-4
SummenformelC8H6BrNO
Durchschnittliche Molmasse212,04 g/mol
Monoisotopische Masse210,96327591 g/mol
SMILESCOc1ccc(Br)c(C#N)c1
InChIKeyZQONVYONOASKIY-UHFFFAOYSA-N
PubChem CID21784096
EC No.625-739-1
DTXSIDDTXSID80617998

Chemische & physikalische Eigenschaften

XLogP2,3
Polarare Oberfläche (TPSA)33
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen1
Schwere Atome11
Formalladung0
Komplexität174
Schmelzpunkt99-102 °C
Siedepunkt292.8±30.0 °C(Predicted)
Dichte1.56±0.1 g/cm3(Predicted)
Lagerbedingungen2-8°C
Aggregatzustandsolid
Farbepeachy
InChIInChI=1S/C8H6BrNO/c1-11-7-2-3-8(9)6(4-7)5-10/h2-4H,1H3
InChIKeyZQONVYONOASKIY-UHFFFAOYSA-N
SMILESC(#N)C1=CC(OC)=CC=C1Br
CAS Datenbank138642-47-4

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (97.8%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 46 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesAcute Tox. 4 (97.8%)
Wassergefährdungsklasse (WGK)3
UN-TransportnummerUN3439
Zollcode29269090
R-Sätze (R)22
GefahrensymboleXn
Sicherheitshinweise (S)36/37
Gefahrenklasse6.1Acute Tox. 4 Oral
VerpackungsgruppeIII
Lagerklasse11 - Combustible Solids

Anwendungen & Verwendung

Verwenden

2-Bromo-5-methoxybenzonitrile (10.0 g, 47.2 mmol) was dissolved in dry tetrahydrofuran (100 mL) in a flame-dried flask and cooled in an ice bath. A solution of borane in tetrahydrofuran (75 mL, 75 mmol, 1.0 M) was added dropwise over 30 minutes. The reaction mixture was stirred overnight at rt, then quenched slowly with ice water and Na2CO3 (saturated aqueous solution). After removing THF, the residue was extracted with large amounts of EtOAc three times. The combined organic layers were washed with water, dried, and concentrated to give the crude, which was purified by silica gel column chromatography to give 1-(2-Bromo-5-methoxyphenyl)methanamine as a white powder (3.65 g, 36%).