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30727-09-4

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30727-09-4 Usage

General Description

Tetrahydrofurfuryl-N,N-dimethylamine is a chemical compound with the molecular formula C8H17NO. It is a tertiary amine and an organic compound that is used as a curing agent in epoxy resin systems. This chemical is known for its ability to provide good mechanical and thermal resistance, making it suitable for a variety of industrial applications. It is also used as a corrosion inhibitor for metal surfaces and as a catalyst in chemical reactions. Tetrahydrofurfuryl-N,N-dimethylamine has low viscosity and good wetting properties, making it an effective and versatile additive in various formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 30727-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,2 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30727-09:
(7*3)+(6*0)+(5*7)+(4*2)+(3*7)+(2*0)+(1*9)=94
94 % 10 = 4
So 30727-09-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO/c1-8(2)6-7-4-3-5-9-7/h7H,3-6H2,1-2H3

30727-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1-(oxolan-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names Furfurylamine,tetrahydro-N,N-dimethyl

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:30727-09-4 SDS

30727-09-4Downstream Products

30727-09-4Relevant articles and documents

A free radical Mannich type reaction: selective α-CH aminomethylation of ethers by Ti(III)/t-BuOOH system under aqueous acidic conditions

Clerici, Angelo,Cannella, Rosalba,Pastori, Nadia,Panzeri, Walter,Porta, Ombretta

, p. 5986 - 5994 (2006)

tert-Butoxy radical, generated by Ti(III)-one electron reduction of tert-butylhydroperoxide, selectively abstracts an α-H atom from ethers. The resulting α-ethereal radicals add to the C-atom of methylene iminium salts, formed in situ under aqueous acidic conditions, leading to a one-pot aminomethylation of ethers at room temperature. The aminoalkylation of ethers is also considered and the role of the metal ion is discussed.

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