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18271-82-4

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18271-82-4 Usage

General Description

2,2,2-trichloro-1-methoxyethanol is a chemical compound that is primarily used as a disinfectant and preservative in a variety of products such as cleaning solutions, cosmetics, and pharmaceuticals. It is a clear, colorless liquid with a mild, ether-like odor. The compound is highly effective at killing a wide range of microorganisms, including bacteria, viruses, and fungi. However, it is also known to be toxic if ingested or inhaled in large amounts, and can cause irritation to the skin, eyes, and respiratory system. Additionally, its use has been restricted in some countries due to concerns about its potential environmental and health impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 18271-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,7 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18271-82:
(7*1)+(6*8)+(5*2)+(4*7)+(3*1)+(2*8)+(1*2)=114
114 % 10 = 4
So 18271-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H5Cl3O2/c1-8-2(7)3(4,5)6/h2,7H,1H3

18271-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trichloro-1-methoxyethanol

1.2 Other means of identification

Product number -
Other names chloral methylhemiacetal

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:18271-82-4 SDS

18271-82-4Relevant articles and documents

Interactive n→σ* delocalizations that control an aqueous organic equilibrium

Fan, Yun-Hua,Haseltine, John

, p. 9279 - 9282 (1996)

Hydrated acetaldehydes were condensed in D2O with substituted alcohols and thiols to determine ΔG of hemiacetalization by 1H NMR. Specific n→σ* delocalizalions in the alkoxy/alkylthio functionality of the product interact to influence n→σ* delocalization in the hemiacetal functionality. Delocalization in the latter functionality controls ΔG.

Lewis Acid Catalysis of Ene Addition of Chloral and Bromal to Olefins; Product Studies

Benner, Jill P.,Gill, G. Bryon,Parrott, Stephen J.,Wallace, Brian

, p. 291 - 313 (2007/10/02)

The addition of chloral and bromal to a variety of alkyl-substituted alkenes has been investigated.The effect of the reaction of varying the Lewis acid catalyst and the structure of substrate have been studied.Anhydrous AlCl3 was found to be most effective catalyst, and ene-type adducts were the major products in most cases.Side reactions were observed with the less reactive systems leading, variously, to the formation of trihalogenoketones, hydrohalogenated ene adducts, and cyclic ethers.Conditions for optimising the yield of ene adducts were established in some cases.The trihalogenoketone by-products can be conveniently removed by a Grignard-type reaction.

Study of the hemiacetals and hemimercaptals of chloral

Hesse,Moll,Augustin

, p. 304 - 314 (2007/10/05)

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