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1475-12-3

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1475-12-3 Usage

General Description

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 and has been found to exhibit strong antibacterial and antifungal properties. It is also a potential building block in the synthesis of various organic compounds. However, caution should be taken when handling 1-(2,5-Dichlorophenyl)ethanol, as it may cause irritation to the skin, eyes, and respiratory system upon exposure.

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 articles and documents

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.

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