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2-bromoethyl 3,4-dimethylphenyl ether is a synthetic chemical compound belonging to the class of organic compounds known as aryl-alkyl ethers. It is characterized by a bromoethyl group attached to an ether functional group and a phenyl ring substituted with two methyl groups at positions 3 and 4. The molecular structure of 2-bromoethyl 3,4-dimethylphenyl ether also exhibits aromatic characteristics. As a laboratory reagent, it is used in specific chemical synthesis or reactions due to its chemical properties. However, it is crucial to handle 2-bromoethyl 3,4-dimethylphenyl ether with care due to potential hazards associated with it.

3351-53-9

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3351-53-9 Usage

Uses

Used in Chemical Synthesis:
2-bromoethyl 3,4-dimethylphenyl ether is used as a laboratory reagent for chemical synthesis, particularly in reactions that require its unique aryl-alkyl ether structure. Its bromoethyl group and methyl-substituted phenyl ring contribute to the formation of various complex organic molecules.
Used in Research Applications:
In the field of organic chemistry, 2-bromoethyl 3,4-dimethylphenyl ether is used as a research compound to study the properties and reactivity of aryl-alkyl ethers. Its molecular structure and aromatic characteristics make it a valuable tool for understanding the behavior of similar compounds in chemical reactions.
Used in Pharmaceutical Industry:
2-bromoethyl 3,4-dimethylphenyl ether may be used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure can be utilized to develop new drugs or improve the properties of existing ones, such as solubility, stability, or bioavailability.
Used in Material Science:
2-bromoethyl 3,4-dimethylphenyl ether may also find applications in material science, where its chemical properties can be exploited to develop new materials with specific characteristics, such as improved thermal stability, electrical conductivity, or mechanical strength.

Check Digit Verification of cas no

The CAS Registry Mumber 3351-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3351-53:
(6*3)+(5*3)+(4*5)+(3*1)+(2*5)+(1*3)=69
69 % 10 = 9
So 3351-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BrO/c1-8-3-4-10(7-9(8)2)12-6-5-11/h3-4,7H,5-6H2,1-2H3

3351-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-bromoethoxy)-1,2-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 2-bromoethyl 3,4-dimethylphenyl ether

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:3351-53-9 SDS

3351-53-9Relevant academic research and scientific papers

Discovery of 1-aryloxyethyl piperazine derivatives as Kv1.5 potassium channel inhibitors (part I)

Guo, Xiaoke,Ma, Xianglei,Yang, Qian,Xu, Jing,Huang, Lu,Jia, Jianmin,Shan, Jiaojiao,Liu, Li,Chen, Weilin,Chu, Hongxi,Wei, Jinlian,Zhang, Xiaojin,Sun, Haopeng,Tang, Yiqun,You, Qidong

supporting information, p. 89 - 94 (2014/06/09)

Kv1.5 potassium channel is an efficacious and safe therapeutic target for the treatment of atrial fibrillation (AF), the most common arrhythmia that threatens human. Herein, by modifying the hit compound 7k from an in-house database, 48 derivatives were synthesized for the assay of their Kv1.5 inhibitory effects by whole cell patch clamp technique. Six compounds which showed better potency than the positive compound dronedarone were selected for the next evaluation of their drug-like properties. Compound 8 exhibited balanced solubility and permeability. It also showed acceptable pharmacodynamics profile with very low acute toxicity. Taking all these data into account, compound 8 can serve as a promising lead for the development of novel therapeutic agent for the treatment of AF.

Phenylacetamide derivatives

-

, (2008/06/13)

A phenylacetamide derivative of formula (I) have potent analgesic and anti-inflammatory activities and exhibit less irritability and toxicity: STR1 wherein, X, Y, W, n, m and Ar are as defined in the specification.

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