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1-(4-BROMOBUTOXY)-4-METHOXY-BENZENE, with the chemical formula C11H15BrO2, is a clear, colorless liquid chemical compound. It has a molecular weight of 255.14 g/mol and features a benzene ring with a methoxy group and a bromobutoxy group attached, which imparts it with unique chemical properties. Due to its potential harmful effects if ingested, inhaled, or causing irritation to the skin and eyes, careful handling is required.

2033-83-2

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2033-83-2 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-BROMOBUTOXY)-4-METHOXY-BENZENE is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties that can be leveraged in the development of various medications.
Used in Organic Chemicals Industry:
1-(4-BROMOBUTOXY)-4-METHOXY-BENZENE also serves as an intermediate in the synthesis of other organic chemicals, where its specific structural features contribute to the formation of desired end products in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 2033-83-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2033-83:
(6*2)+(5*0)+(4*3)+(3*3)+(2*8)+(1*3)=52
52 % 10 = 2
So 2033-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BrO2/c1-13-10-4-6-11(7-5-10)14-9-3-2-8-12/h4-7H,2-3,8-9H2,1H3

2033-83-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromobutoxy)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 1-(4-methoxyphenoxy)-4-bromobutane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2033-83-2 SDS

2033-83-2Relevant academic research and scientific papers

A pillar[5]arene-based cyanide sensor bearing on a novel cyanide-induced self-assemble mechanism

Cheng, Xiaobin,Li, Hui,Zheng, Feng,Lin, Qi,Zhang, Youming,Yao, Hong,Wei, Taibao

, p. 59 - 66 (2016)

We have designed and synthesized a novel copillar[5]arene-based chemosensor, which employ 8-hydroxyquinoline group as a binding site and signal group. By a novel cyanide-induced self-assemble mechanism, the pillar[5]arene-based chemosensor shown high sens

Photoresponsive supramolecular self-assembly of monofunctionalized pillar[5]arene based on stiff stilbene

Wang, Yuan,Xu, Jiang-Fei,Chen, Yu-Zhe,Niu, Li-Ya,Wu, Li-Zhu,Tung, Chen-Ho,Yang, Qing-Zheng

, p. 7001 - 7003 (2014)

We report a photoresponsive monofunctionalized pillar[5]arene based on stiff stilbene. The Z isomer, Z-1, tends to form self-complexing [1]pseudorotaxanes and [c2] daisy chains, whereas the E analog, E-1, forms supramolecular polymers. the Partner Organis

Stimuli-responsive supramolecular polymer network based on bi-pillar[5]arene for efficient adsorption of multiple organic dye contaminants

Wei, Tai-Bao,Qi, Li-Hua,Zhang, Qin-Peng,Zhang, Wen-Huan,Yao, Hong,Zhang, You-Ming,Lin, Qi

, p. 12531 - 12537 (2020)

A novel supramolecular polymer network gel (NT), based on bi-pillar[5]arene, which can adsorb and separate organic dyes, has been efficiently constructed. First, a novel supramolecular gelator, NBP5 (host), and a tripodal guest, TG (guest), were successfu

A stretchable pillararene-containing supramolecular polymeric material with self-healing property

Chen, Jianzhuang,Han, Huijing,Li, Changjun,Liao, Xiaojuan,Shan, Xiaotao,Xie, Meiran,Zhao, Meng,Zhao, Qiuhua

supporting information, (2021/05/25)

Constructing polymeric materials with stretchable and self-healing properties arise increasing interest in the field of tissue engineering, wearable electronics and soft actuators. Herein, a new type of supramolecular cross-linker was constructed through

Tumor microenvironment responsive supramolecular glyco-nanovesicles based on diselenium-bridged pillar[5]arene dimer for targeted chemotherapy

Chen, Zelong,Hu, Xianjun,Jin, Ming,Pei, Yuxin,Pei, Zhichao,Pu, Liang,Wang, Yang

supporting information, p. 10642 - 10645 (2020/10/02)

Supramolecular glyco-nanovesicles (SeSe-(P5)2?Man-NH3+) based on the host-guest complex of a diselenium-bridged pillar[5]arene dimer and a mannose derivative have been successfully developed for the first time, which possessed tumor microenvironment-respo

Dual-Stimuli-Responsive Fluorescent Supramolecular Polymer Based on a Diselenium-Bridged Pillar[5]arene Dimer and an AIE-Active Tetraphenylethylene Guest

Wang, Yan,Lv, Ming-Zhe,Song, Nan,Liu, Zeng-Jie,Wang, Chunyu,Yang, Ying-Wei

, p. 5759 - 5766 (2017/08/14)

We report a new strategy to construct a multi-stimuli-responsive fluorescent supramolecular polymer by the strong host-guest interactions between a diselenium bond-bridged pillar[5]arene dimer and an AIE-active tetraphenylethylene (TPE)-containing neutral

Efficacy of novel phenoxyalkyl pyridinium oximes as brain-penetrating reactivators of cholinesterase inhibited by surrogates of sarin and VX

Chambers, Janice E.,Chambers, Howard W.,Funck, Kristen E.,Meek, Edward C.,Pringle, Ronald B.,Ross, Matthew K.

, p. 154 - 159 (2016/12/06)

Pyridinium oximes are strong nucleophiles and many are effective reactivators of organophosphate-inhibited cholinesterase (ChE). However, the current oxime reactivators are ineffective at crossing the blood-brain barrier and reactivating brain ChE in the intact organism. Our laboratories have developed a series of substituted phenoxyalkyl pyridinium oximes (US patent 9,227,937 B2) with the goal of identifying reactivators effective in crossing the blood-brain barrier. The first 35 of the series were found to have similar in?vitro efficacy as reactivators of ChE inhibited by a sarin surrogate (phthalimidyl isopropyl methylphosphonate, PIMP) or a VX surrogate (nitrophenyl ethyl methylphosphonate, NEMP) in bovine brain preparations as previously observed in rat brain preparations. A number of these novel oximes have shown the ability to decrease the level of ChE inhibition in the brains of rats treated with a high sublethal dosage of either a sarin surrogate (nitrophenyl isopropyl methylphosphonate, NIMP) or the VX surrogate NEMP. Levels of reactivation at 2?h after oxime administration were up to 35% while the currently approved therapeutic, 2-PAM, yielded no reduction in brain ChE inhibition. In addition, there was evidence of attenuation of seizure-like behavior with several of the more effective novel oximes, but not 2-PAM. Therefore these novel oximes have demonstrated an ability to reactivate inhibited ChE in brain preparations from two species and in?vivo data support their ability to enter the brain and provide a therapeutic action. These novel oximes have the potential to be developed into improved antidotes for nerve agent therapy.

Synthesis and cytotoxicity of 2,3-enopyranosyl C-linked conjugates of genistein

Szeja, Wieslaw,Grynkiewicz, Grzegorz,Bieg, Tadeusz,Swierk, Piotr,Byczek, Anna,Papaj, Katarzyna,Kitel, Radoslaw,Rusin, Aleksandra

, p. 7072 - 7093 (2014/07/08)

A series of glycoconjugates, derivatives of genistein containing a C-glycosylated carbohydrate moiety, were synthesized and their anticancer activity was tested in vitro in the human cell lines HCT 116 and DU 145. The target compounds 15-17 were synthesiz

Synthesis of N-aryloxyalkylanabasine derivatives

Slyn'Ko,Tatarova,Shakirov,Shul'Ts

, p. 294 - 301 (2013/07/26)

N-Aryloxyalkylanabasine derivatives were prepared via the reaction of anabasine hydrochloride with various aryloxyhaloalkanes in the presence of potash in DMF. The reaction occurred with retention of the chiral center C-(2) of the piperidine group. Side products of bis(aryloxy)ethanes were characterized.

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