1211514-99-6 Usage
Substituted benzene derivative
A benzene ring with various functional groups attached, altering its chemical properties.
Methoxy group
An oxygen atom bonded to a methyl group (-OCH3), contributing to the compound's polarity.
Bromine atom
A halogen atom (Br) attached to the benzene ring, which can increase the compound's reactivity and molecular weight.
Pentafluorosulfanyl group
A fluorinated sulfur atom (SF5) attached to the benzene ring, providing unique properties such as high electronegativity and lipophilicity.
Colorless liquid
The compound's physical state and appearance, which can affect its handling and storage.
Building block in organic synthesis
A precursor compound used to create more complex molecules in organic chemistry.
Applications in pharmaceuticals, agrochemicals, and materials science
The various industries in which 1-Methoxy-2-bromo-4-(pentafluorosulfanyl)benzene can be utilized for the development of new products.
Unique and valuable properties of the pentafluorosulfanyl group
The group's high electronegativity and lipophilicity can enhance the compound's effectiveness in various applications.
Hazardous if not properly managed
The presence of the bromine atom requires careful handling to avoid potential hazards and risks.
Check Digit Verification of cas no
The CAS Registry Mumber 1211514-99-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,1 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1211514-99:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*1)+(3*4)+(2*9)+(1*9)=106
106 % 10 = 6
So 1211514-99-6 is a valid CAS Registry Number.
1211514-99-6Relevant articles and documents
Pentafluorosulfanyl-Substituted Benzopyran Analogues As New Cyclooxygenase-2 Inhibitors with Excellent Pharmacokinetics and Efficacy in Blocking Inflammation
Zhang, Yanmei,Wang, Yican,He, Chuang,Liu, Xiaorong,Lu, Yongzhi,Chen, Tingting,Pan, Qiong,Xiong, Jingfang,She, Miaoqin,Tu, Zhengchao,Qin, Xiaochu,Li, Minke,Tortorella, Micky D.,Talley, John J.
, p. 4135 - 4146 (2017)
In this report, we disclose the design and synthesis of a series of pentafluorosulfanyl (SF5) benzopyran derivatives as novel COX-2 inhibitors with improved pharmacokinetic and pharmacodynamic properties. The pentafluorosulfanyl compounds showe
Five sulfur hexafluoride substituted benzo-type compounds and use thereof
-
, (2018/10/11)
The invention discloses a sulfur pentafluoride-substituted benzopyran compound shown in the structural formula I or its pharmaceutically acceptable salt or stereoisomer or prodrug molecule. The sulfur pentafluoride-substituted benzopyran compound has effe
SNAr reactions of nitro-(pentafluorosulfanyl)benzenes to generate SF5 aryl ethers and sulfides
Beier, Petr,Pastyrikova, Tereza,Vida, Norbert,Iakobson, George
, p. 1466 - 1469 (2011/06/09)
Nucleophilic aromatic substitution of the nitro group of para- and meta-nitro-(pentafluorosulfanyl)benzene with alkoxides and thiolates generates a range of substituted 4- and 3-(pentafluorosulfanyl)benzenes in a single-step reaction.
