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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 77014생성일: 2026년 10월 26일

1-Bromo-4-(methylsulphonyl)benzene

4-Bromophenyl · NSC 174742 · TIMTEC-BB SBB006294 · 4-Bromo phenyl methyl · 4-BROMOPHENYL METHYL SULFON · Methyl 4-Bromophenylsulfone · 4-Bromophenyl methylesulfone · P-METHYL BENZENESULFOBROMIDE

https://huagongshe.com/ko/chemical/77014

1-Bromo-4-(methylsulphonyl)benzene 분자 구조식

식별자 및 물리적 특성

CAS No.3466-32-8
분자식C7H7BrO2S
평균 분자량235.1 g/mol
단동위원소 질량233.93501256 g/mol
SMILESCS(=O)(=O)c1ccc(Br)cc1
InChIKeyFJLFSYRGFJDJMQ-UHFFFAOYSA-N
PubChem CID77014
EC No.222-421-0
DTXSIDDTXSID20188218

화학 및 물리적 성질

XLogP1.1
극성 표면적42.5
수소 결합 공여자 수0
수소 결합 수용자 수2
회전 가능 결합 수1
무거운 원자 수11
형식 전하0
복잡도209
녹는점103-107 °C (lit.)
끓는 점348.6±34.0 °C(Predicted)
밀도1.595±0.06 g/cm3(Predicted)
저장 조건Store at room temperature
용해도메탄올에 용해됨
물리적 상태결정 또는 결정성 분말
색상하얀색
BRN2045675
InChIInChI=1S/C7H7BrO2S/c1-11(9,10)7-4-2-6(8)3-5-7/h2-5H,1H3
InChIKeyFJLFSYRGFJDJMQ-UHFFFAOYSA-N
SMILESC1(Br)=CC=C(S(C)(=O)=O)C=C1

화학적 성질

Whitetolightyellowcrystalspowe

안전 및 규제

GHS 분류WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, 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 8 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
수질 위해 등급(WGK)3
관세 코드29309090
위험 문구(R)22-36/37/38
위험 표시Xn,Xi
안전 문구(S)22-24/25-36/37/39-26
위험 참고 사항Irritant
저장 분류11 - Combustible Solids

용도

용도

4-Bromophenyl methyl sulfone may be used to synthesize:biaryl methyl sulfones5-[[-4-(methylsulfonyl)phenyl]thio]thiophene-2-sulfonamide1-[4-(methylsulfonyl)phenyl]-1H-pyrazole (Hmsppz)DuP 697 via reaction with (5-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)trimethylsilane4-Bromophenyl methyl sulfone (1-bromo-4-(methylsulfonyl)benzene) can undergo coupling reaction with benzene sulfonamide in the presence of copper(I)iodide to form the corresponding N-aryl sulfonamide.