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142647-87-8

N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Phenol, 2,2',2'',2'''-[1,2-ethanediylbis[nitrilobis(methylene)]]tetrakis[4,6-dimethyl-

    Cas No: 142647-87-8

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  • 142647-87-8 Structure

  • Basic information

    1. Product Name: N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine
    2. Synonyms: N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine
    3. CAS NO:142647-87-8
    4. Molecular Formula: C38H48 N2 O4
    5. Molecular Weight: 596.7987
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142647-87-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 708.2°Cat760mmHg
    3. Flash Point: 342.2°C
    4. Appearance: /
    5. Density: 1.172g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine(142647-87-8)
    11. EPA Substance Registry System: N,N,N',N'-tetrakis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine(142647-87-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 142647-87-8(Hazardous Substances Data)

142647-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142647-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,6,4 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142647-87:
(8*1)+(7*4)+(6*2)+(5*6)+(4*4)+(3*7)+(2*8)+(1*7)=138
138 % 10 = 8
So 142647-87-8 is a valid CAS Registry Number.

142647-87-8SDS

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-[[2-[bis[(2-hydroxy-3,5-dimethylphenyl)methyl]amino]ethyl-[(2-hydroxy-3,5-dimethylphenyl)methyl]amino]methyl]-4,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names Thm2BED

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:142647-87-8 SDS

142647-87-8Downstream Products

142647-87-8Relevant articles and documents

Molecular assembly of highly symmetric molecules under a hydrogen bond framework controlled by alkyl building blocks: A simple approach to fine-tune nanoscale structures

Tanphibal, Pimsai,Tashiro, Kohji,Chirachanchai, Suwabun

, p. 486 - 491 (2016/01/09)

To date, molecular assemblies under the contribution of hydrogen bond in combination with weak interactions and their consequent morphologies have been variously reported; however, how the systematic variation of the structure can fine-tune the morphologi

Synthesis and characterization of magnesium alkoxides incorporated into bulky aluminium tetraphenolate helices and application in the ring-opening polymerization of lactides

Jian, Chunli,Zhang, Jinjin,Dai, Zhongran,Gao, Yuan,Tang, Ning,Wu, Jincai

, p. 3533 - 3541 (2013/07/26)

Two aluminium and magnesium heterobimetallic complexes of [(LAl)MgOBn] 2 (2) and [(LAl)Mg(OC2H4OCH3)] 2 (3), in which L = N1,N1,N2,N 2-tetrakis(2-hydroxy-3,

Synthesis and structure of aluminium amine-phenolate complexes

Johnson, Andrew L.,Davidson, Matthew G.,Perez, Yolanda,Jones, Matthew D.,Merle, Nicolas,Raithby, Paul R.,Richards, Stephen P.

scheme or table, p. 5551 - 5558 (2009/12/23)

Reaction of Al(OiPr)3 with the tris-phenol amine ligand L1H3 in toluene at ambient temperature results in the formation of the iso-propanol adduct [HOiPr·Al(L 1)]. Single crystal X-ray diff

Multidentate aminophenol ligands prepared with Mannich condensations

Higham, Christine S.,Dowling, Daniel P.,Shaw, Janet L.,Cetin, Anil,Ziegler, Christopher J.,Farrell, Joshua R.

, p. 4419 - 4423 (2007/10/03)

Mannich condensations were used to prepare a series of multidentate aminophenol compounds from ethylenediamine, various amounts of paraformaldehyde and 2,4-disubstituted phenols. One of these diaminotetraphenol compounds was reacted with Zn(OAc)2/su

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