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Benzenemethanol, 4-(2-bromoethoxy)-, also known as 4-(2-bromoethoxy)benzenemethanol or 4-(2-bromoethyl)phenylmethanol, is an organic compound with the chemical formula C8H9BrO. It is a colorless liquid at room temperature and has a molecular weight of 201.06 g/mol. Benzenemethanol, 4-(2-bromoethoxy)- is characterized by the presence of a benzene ring with a hydroxyl group (-OH) attached to the 4-position and a 2-bromoethoxy group (-OCH2CH2Br) attached to the same position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its reactivity, it is important to handle Benzenemethanol, 4-(2-bromoethoxy)- with care, as it may pose health risks and environmental concerns.

38459-72-2

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38459-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38459-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,5 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38459-72:
(7*3)+(6*8)+(5*4)+(4*5)+(3*9)+(2*7)+(1*2)=152
152 % 10 = 2
So 38459-72-2 is a valid CAS Registry Number.

38459-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2-bromoethoxy)phenyl]methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,4-(2-bromoethoxy)

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:38459-72-2 SDS

38459-72-2Relevant academic research and scientific papers

A New Chiral Cyclophane Derived from 1,1'-Binaphthol and Benzylviologen

Deng, Nanlin,Marwaha, Vijay Rai,Garcia, Maurie E.,Benesi, Alan,Mallouk, Thomas E.

, p. 7599 - 7602 (1995)

A new chiral cyclophane, with a binding cavity defined by the 1,1'-binaphthyl "minor groove" and a strongly ?-accepting 4,4'-bipyridinium dication, has been synthesized.It self-associates in solution (K=(4.1+/-1.6)*102 M-1), and forms charge-transfer complexes with strong ?-electron donors.

HYPOXANTHINE COMPOUND

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, (2021/07/17)

PROBLEM TO BE SOLVED: To provide a novel compound having an inhibitory action of prolyl hydroxylase (PHDs) and useful as a therapeutic agent of an inflammatory bowel disease such as ulcerative colitis. SOLUTION: The present invention relates to a hypoxanthine compound represented by the following formula (I) or a pharmacologically acceptable salt thereof. The compound of the present invention or its pharmaceutically acceptable salt has an inhibitory effect of prolyl hydroxylase and is useful as a therapeutic agent for inflammatory bowel disease such as ulcerative colitis. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Design, synthesis, in silico and in vitro studies for new nitric oxide‐releasing indomethacin derivatives with 1,3,4‐oxadiazole‐2‐thiol scaffold

Sava, Alexandru,Buron, Frederic,Routier, Sylvain,Panainte, Alina,Bibire, Nela,Constantin, Sandra M?d?lina,Lupa?cu, Florentina Geanina,Foc?a, Alin Viorel,Profire, Lenu?a

, (2021/07/07)

Starting from indomethacin (IND), one of the most prescribed non‐steroidal anti‐inflammatory drugs (NSAIDs), new nitric oxide‐releasing indomethacin derivatives with 1,3,4‐oxadiazole‐ 2‐thiol scaffold (NO‐IND‐OXDs, 8a‐p) have been developed as a safer and

Preparation method and application of naphthylamine compounds and salts thereof

-

, (2020/08/30)

The invention discloses a preparation method and application of naphthylamine compounds and salts thereof, concretely provides a method for synthesizing the naphthylamine compounds by taking 4-formylphenol as a substrate, and also provides a preparation m

Naphthylamine compound and biologically acceptable salt thereof as well as preparation method and application thereof

-

Paragraph 0128; 0145-0147, (2019/12/15)

Aiming at shortage of anti-cancer targeting medicines in the prior art, the invention provides a naphthylamine compound and a biologically acceptable salt thereof as well as a preparation method and application thereof. By adopting the naphthylamine compo

USE OF DISUBSTITUTED BENZENES TO CONTROL INSECTICIDE-RESISTANT PESTS

-

Page/Page column 35; 36; 39; 40, (2018/11/26)

The invention is in the technical field of insect control and relates to the use of a disubstituted benzenes for controlling insecticide-resistant pests such as mosquitoes and cockroaches.

PHENYL BENZYL ETHER DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOF

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Paragraph 0145; 0158, (2017/06/12)

Parts of compounds, after being labeled by radionuclide, of the phenyl benzyl ether derivative, are used as Aβ plaque imaging agent. The structural formula of the phenyl benzyl ether derivative is shown by formula (I). The present invention develops a kin

Synthesis and evaluation of 2-nonylaminopyridine derivatives as PPAR ligands

Usui, Shinya,Fujieda, Hiroki,Suzuki, Takayoshi,Yoshida, Naoaki,Nakagawa, Hidehiko,Ogura, Michitaka,Makishima, Makoto,Miyata, Naoki

, p. 1053 - 1059 (2008/02/12)

To find novel PPAR ligands, we prepared several 3-{3 or 4-[2-(nonylpyridin-2-ylamino)ethoxy]phenyl}-propanoic acid derivatives which were designed based on the structure of our previous PPARγ ligand 1. In PPAR binding affinity assays, compound 4, which ha

INSECTICIDAL HETEROCYCLIC 1,4-DISUBSTITUTED BENZENE N-OXIDES

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Page/Page column 12; 27, (2008/06/13)

Certain novel heterocyclic 1,4-disubstituted benzene N-oxide derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula (I) wherein R1, R2, B, D, T, U, m, and n are fully des

Benzothieno[3,2-b]indole derivatives as potent selective estrogen receptor modulators

Ji, Qinggang,Gao, Jie,Wang, Junbo,Yang, Chunhao,Hui, Xin,Yan, Xueming,Wu, Xihan,Xie, Yuyuan,Wang, Ming-Wei

, p. 2891 - 2893 (2007/10/03)

A series of estrogen receptor ligands based on benzothieno[3,2-b]indole were synthesized and their binding affinity for estrogen receptor subtypes (ERα and ERβ) and effects on mouse uterus and bone were evaluated. Some of these compounds showed strong bin

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