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Cyclohexane, 1,1-diethoxy-2-methyl- is an organic compound with the chemical formula C10H20O2. It is a colorless liquid with a density of 0.87 g/cm3 and a boiling point of 180-181°C. Cyclohexane, 1,1-diethoxy-2-methyl- is a derivative of cyclohexane, featuring a methyl group at the 2-position and two ethoxy groups attached to the 1-position. It is used as a solvent, a chemical intermediate in the synthesis of various organic compounds, and in the production of pharmaceuticals and agrochemicals. Due to its potential health and environmental hazards, it is important to handle this substance with care and follow proper safety guidelines.

1528-18-3

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1528-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1528-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1528-18:
(6*1)+(5*5)+(4*2)+(3*8)+(2*1)+(1*8)=73
73 % 10 = 3
So 1528-18-3 is a valid CAS Registry Number.

1528-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methylcyclohexanone diethyl acetal

1.2 Other means of identification

Product number -
Other names 2-Methyl-cylohexanon-diaethylketal

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:1528-18-3 SDS

1528-18-3Relevant academic research and scientific papers

Iron(III) tosylate in the preparation of dimethyl and diethyl acetals from ketones and β-keto enol ethers from cyclic β-diketones

Mansilla, Horacio,Afonso, Maria M.

, p. 2607 - 2618 (2008/12/22)

An efficient method for conversion of ketones to their corresponding dimethyl and diethyl acetals and of cyclic β-diketones into β-keto enol ethers using Fe(OTs)3 as a catalyst is described. Copyright Taylor & Francis Group, LLC.

A simple, one-flask transformation of ketones to N-methyl lactams

Hoffman, Robert V.,Salvador, James M.

, p. 2429 - 2432 (2007/10/02)

A one-flask conversion of cyclic ketones to N-methyl lactams is described. Reaction of the ketone with triethylorthoformate generates an acetal which is reacted in situ with N-(((p-nitrobenzene)sulfonyl)oxy methylamine 2a(CH3NH-OSO2C6H4NO2). Dealkylation of the resulting O-ethyl imidate with sodium iodide gives the lactam. A variety of lactams, including macrocyclic lactams, are produced simply and in good yields.

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