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1-(2,5-Dichlorophenyl)ethanol, also known as 2,5-dichlorophenylethanol, is a chemical compound with the molecular formula C8H8Cl2O. It is a white to off-white solid with a faint odor and is commonly used in the production of pharmaceuticals and pesticides. 1-(2,5-DICHLOROPHENYL)ETHANOL has been studied for its potential as an antimicrobial agent, exhibiting strong antibacterial and antifungal properties. It also serves as a potential building block in the synthesis of various organic compounds. However, due to its potential to cause irritation to the skin, eyes, and respiratory system upon exposure, caution should be exercised during handling.

1475-12-3

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1475-12-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(2,5-DICHLOROPHENYL)ETHANOL is used as an active ingredient for its antimicrobial properties, particularly in the development of antibiotics and antifungal medications. Its strong antibacterial and antifungal properties make it a valuable component in creating effective treatments against various infections.
Used in Pesticide Industry:
1-(2,5-DICHLOROPHENYL)ETHANOL is used as a key component in the formulation of pesticides, leveraging its antimicrobial properties to control and eliminate pests. This application helps protect crops and maintain agricultural productivity.
Used in Organic Synthesis:
1-(2,5-DICHLOROPHENYL)ETHANOL is used as a building block in the synthesis of various organic compounds. Its unique chemical structure allows it to be a versatile intermediate in the creation of a wide range of chemical products, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Antimicrobial Applications:
1-(2,5-DICHLOROPHENYL)ETHANOL is used as an antimicrobial agent for its strong antibacterial and antifungal properties. It can be incorporated into various products, such as disinfectants, sanitizers, and preservatives, to ensure cleanliness and prevent the spread of harmful microorganisms.

Check Digit Verification of cas no

The CAS Registry Mumber 1475-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1475-12:
(6*1)+(5*4)+(4*7)+(3*5)+(2*1)+(1*2)=73
73 % 10 = 3
So 1475-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O/c1-5(11)7-4-6(9)2-3-8(7)10/h2-5,11H,1H3

1475-12-3SDS

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-(2,5-Dichlorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-(2,5-Dichlorophenyl)ethanol

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:1475-12-3 SDS

1475-12-3Relevant academic research and scientific papers

Transformation of Alkynes into Chiral Alcohols via TfOH-Catalyzed Hydration and Ru-Catalyzed Tandem Asymmetric Hydrogenation

Liu, Sensheng,Liu, Huan,Zhou, Haifeng,Liu, Qixing,Lv, Jinliang

supporting information, p. 1110 - 1113 (2018/02/23)

A novel full atom-economic process for the transformation of alkynes into chiral alcohols by TfOH-catalyzed hydration coupled with Ru-catalyzed tandem asymmetric hydrogenation in TFE under simple conditions has been developed. A range of chiral alcohols was obtained with broad functional group tolerance, good yields, and excellent stereoselectivities.

Development of a novel chiral palladacycle and its application in asymmetric hydrophosphination reaction

Yap, Jeanette See Leng,Li, Bin Bin,Wong, Jonathan,Li, Yongxin,Pullarkat, Sumod A.,Leung, Pak-Hing

, p. 5777 - 5784 (2014/04/03)

A novel amine ligand, 1-(2,5-dichlorophenyl)-N,N-dimethylethanamine, was synthesized from 1-(2,5-dichlorophenyl)ethanone via a three step synthetic route. Direct ortho-palladation of the amine ligand with Pd(OAc)2 gave the racemic dimeric compl

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