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2-(methoxymethyl)-1,3-dioxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75025-18-2

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75025-18-2 Usage

Type of compound

Cyclic ether

Structural components

Dioxane ring, methoxymethyl group

Common uses

Solvent, reagent in chemical reactions, manufacture of pharmaceuticals and agrochemicals, production of flavors and fragrances

Volatility

Relatively low

Stability

Stable under normal conditions

Industrial applications

Suitable for various applications due to low volatility and stability

Safety precautions

Can be harmful if ingested or inhaled, may cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 75025-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,2 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75025-18:
(7*7)+(6*5)+(5*0)+(4*2)+(3*5)+(2*1)+(1*8)=112
112 % 10 = 2
So 75025-18-2 is a valid CAS Registry Number.

75025-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methoxymethyl)-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 2-methoxymethyl-1,3-dioxane

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:75025-18-2 SDS

75025-18-2Downstream Products

75025-18-2Relevant academic research and scientific papers

Preparation of cyclic 6-membered to 8-membered vinylene-1,2-dioxy compounds

-

, (2008/06/13)

Cyclic 6-membered to 8-membered 1,2-vinylenedioxy compounds of the general formula I STR1 where A is STR2 R1 to R7 independently of one another are each hydrogen, C1 -C8 -alkyl, C2 -C16 -alkoxyalkyl, C2 -C8 -alkenyl, C2 -C8 -alkynyl, C5 -C8 -cycloalkyl, aryl, C7 -C10 -alkylphenyl, C7 -C10 -phenalkyl, C8 -C10 -phenalkenyl or a heterocyclic structure, or R2 and R3, R2 and R4, R3 and R4, R2 and R6, R3 and R6, R4 and R5 or R6 and R7 together form a cycloaliphatic or heterocyclic ring, and R1 to R7 may furthermore carry substituents which are inert under the reaction conditions, and n is 0 or 1, are prepared by a process in which a cyclic 2-oxymethyl-1,3-dioxa compound or one of its derivatives of the general formula II STR3 where R1 to R7, A and n have the abovementioned meanings, and R8 is hydrogen or C1 -C12 -alkyl, is converted in the presence of an acidic catalyst at from 150° to 450° C. and under from 0.001 to 50 bar, some of the compounds obtained being novel.

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