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HCID 59856477생성일: 2026년 10월 28일

Dichloro(1,3-dimesityl-2-imidazolidinylidene)(5-(dimethylsulfamoyl)-2-isopropoxybenzylidene)ruthenium

ZHAN CATALYST-1B · Zhan catalyst · 1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene[2-(iso-propoxy)-5-(N,N-dimethylaminosulfonyl)phenyl]methylene ruthenium(II) dichloride · Dichloride Zhan catalyst 1B · TB-1840 · CATALYST -1B · Dichloro(1,3-dimesityl-2-imidazolidinylidene)[5-(dimethylsulfamoyl)-2-isopropoxybenzylidene]ruthenium · (1,3-Dimesitylimidazolidin-2-ylidene)[5-(N,N-dimethylsulfamoyl)-2-isopropoxybenzylidene]ruthenium(VI) Chloride

https://huagongshe.com/ko/chemical/59856477

Dichloro(1,3-dimesityl-2-imidazolidinylidene)(5-(dimethylsulfamoyl)-2-isopropoxybenzylidene)ruthenium 분자 구조식

식별자 및 물리적 특성

CAS No.918870-76-5
분자식C33H43Cl2N3O3RuS
평균 분자량733.8 g/mol
단동위원소 질량733.144559 g/mol
SMILESCc1cc(C)c(N2CCN(c3c(C)cc(C)cc3C)[C]2=[Ru]([Cl])([Cl])=[CH]c2cc(S(=O)(=O)N(C)C)ccc2OC(C)C)c(C)c1
InChIKeyOXLURKCRXVAJQS-UHFFFAOYSA-L
PubChem CID59856477
EC No.813-485-6

화학 및 물리적 성질

극성 표면적61.5
수소 결합 공여자 수0
수소 결합 수용자 수6
회전 가능 결합 수7
무거운 원자 수43
형식 전하0
복잡도1,130
저장 조건2-8°C, stored under nitrogen
물리적 상태고체
색상녹색
InChIKeyJIZPWEVWTYCVNK-UHFFFAOYSA-L
SMILES[Cl-][Ru+6]1(=[C-2]C2=CC(S(=O)(=O)N(C)C)=CC=C2O1C(C)C)(=[C-2]1N(C2C(=CC(C)=CC=2C)C)CCN1C1C(=CC(C)=CC=1C)C)[Cl-]

안전 및 규제

GHS 분류WarningH302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, 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 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesAcute Tox. 4 (50%)
수질 위해 등급(WGK)3
위험 문구(R)36/37/38
위험 표시Xi
안전 문구(S)26
저장 분류13 - Non Combustible Solids

용도

용도

Zhan Catalyst-1B (Hoveyda-Grubbs type catalyst) can be used:In the preparation of hybrid olefin metathesis catalysts, with increased catalytic activity via immobilization on molecular seives. supportsAs a catalyst in the synthesis of divergent dendrimerIn ring-closure metathesis (RCM) reaction.