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HCID 190026Erstellt: 27. Oktober 2026

Methanesulfonyl bromide

Methanesulfonyl bromide (6CI,7CI,9CI)

https://huagongshe.com/de/chemical/190026

Molekülstruktur von Methanesulfonyl bromide

Identifikatoren & physikalische Daten

CAS No.41138-92-5
SummenformelCH3BrO2S
Durchschnittliche Molmasse159 g/mol
Monoisotopische Masse157,90371 g/mol
SMILESCS(=O)(=O)Br
InChIKeyITYJDNHFRZSTJY-UHFFFAOYSA-N
PubChem CID190026
EC No.628-454-0
DTXSIDDTXSID50276697

Chemische & physikalische Eigenschaften

XLogP0,6
Polarare Oberfläche (TPSA)42,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen0
Schwere Atome5
Formalladung0
Komplexität95
Siedepunkt72-73 °C(Press: 15 Torr)
Dichte1.954 g/mL at 20 °C(lit.)
Brechungsindexn20/D 1.510

Sicherheit & Vorschriften

GHS-EinstufungDangerH300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]H330 (100%): Fatal if inhaled [Danger Acute toxicity, inhalation]P260, P264, P270, P271, P280, P284, P301+P316, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P320, P321, P330, P363, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Hazard Classes and CategoriesAcute Tox. 2 (100%)Skin Corr. 1A (100%)
F8-10-21
Wassergefährdungsklasse (WGK)3
UN-TransportnummerUN 3390 6.1/PG 1
R-Sätze (R)26/28-35
GefahrensymboleT+
Sicherheitshinweise (S)26-28-36/37/39-45

Anwendungen & Verwendung

Verwenden

Methanesulfonyl Bromide is a reagent used for research purposed. Methanesulfonyl Bromide has been applied in 1,3 dipolar cycloaddition reactions to produce fused compound required for DNA binding studies