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19900-69-7

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19900-69-7 Usage

Chemical Properties

4,4'-METHYLENEBIS(2,6-DIISOPROPYLANILINE) is solidified melt

Uses

4,4'-METHYLENEBIS(2,6-DIISOPROPYLANILINE) is an excellent chain extender for elastomeric polyurethanes (PU) especially useful in systems cured at room temperature. It is also a curing agent for epoxides (EP) and an intermediate for organic syntheses.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 19900-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,0 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19900-69:
(7*1)+(6*9)+(5*9)+(4*0)+(3*0)+(2*6)+(1*9)=127
127 % 10 = 7
So 19900-69-7 is a valid CAS Registry Number.

19900-69-7SDS

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 4-[[4-amino-3,5-di(propan-2-yl)phenyl]methyl]-2,6-di(propan-2-yl)aniline

1.2 Other means of identification

Product number -
Other names 4,4'-methylenebis(N-salicylidene-2,6-diisopropylaniline)

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:19900-69-7 SDS

19900-69-7Relevant articles and documents

Highly regioselective para-methylthiolation/bridging methylenation of arylamines promoted by NH4I

Xu, Yinfeng,Cong, Tiantian,Liu, Ping,Sun, Peipei

supporting information, p. 9742 - 9745 (2015/10/05)

Aryl methyl thioethers and methylene-bridged arylamines were synthesized via highly regioselective para-methylthiolation/bridging methylenation of arylamines using DMSO as the methylthio or methylene source in the presence of NH4I under metal-free conditions. For the substrates with both electron-donating and electron-withdrawing substituents, the reaction proceeded smoothly and gave moderate to good yields.

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