N,N'-Diisopropylacetimidamide

Base Information

• Chemical Name: N,N'-Diisopropylacetimidamide
• CAS No.: 106500-93-0
• Molecular Formula: C8H18N2
• Molecular Weight: 142.244
• DSSTox Substance ID: DTXSID40458602
• Nikkaji Number: J1.198.683H
• Mol file: 106500-93-0.mol

Synonyms:N,N'-Diisopropylacetimidamide;106500-93-0;Ethanimidamide, N,N'-bis(1-methylethyl)-;N,N'-di(propan-2-yl)ethanimidamide;N,N'-Bis(1-methylethyl)ethanimidamide;n,n'-diisopropylacetamidine;SCHEMBL838880;SCHEMBL22172310;DTXSID40458602;AMY19329;BBL103121;MFCD19217938;STL556931;AKOS006355057;AKOS030228767;BS-18956;(E)-N,N'-bis(propan-2-yl)ethanimidamide;EthaniMidaMide,N,N'-bis(1-Methylethyl)-;(1E)-N,N'-di(propan-2-yl)ethanimidamide;A935266

Chemical Property of N,N'-Diisopropylacetimidamide

Chemical Property:

• XLogP3: 1.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 142.146998583
• Heavy Atom Count: 10
• Complexity: 114

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NC(=NC(C)C)C

Technology Process of N,N'-Diisopropylacetimidamide

There total 6 articles about N,N'-Diisopropylacetimidamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

triphenylsilanethiol (14606-42-9) + cadmium bis-N,N-diisopropylacetamidinate → C26H32CdN2SSi + N,N'-bis(isopropyl)ethanimidamide (106500-93-0)

Guidance literature:

In toluene; at 20 ℃; for 1h;

DOI:10.1021/acs.inorgchem.0c03307

Reference yield: 80.0%

Trimethyl orthoacetate (1445-45-0) + isopropylamine (75-31-0) → N,N'-bis(isopropyl)ethanimidamide (106500-93-0)

Guidance literature:

Trimethyl orthoacetate; isopropylamine; With acetic acid; for 12h; Heating / reflux;

With sodium methylate; In methanol; n-heptane; at 20 ℃; for 1h;

Reference yield: 57.0%

N,N,N,N,-tetramethylethylenediamine (110-18-9) + triphenylsilanethiol (14606-42-9) + cadmium bis-N,N-diisopropylacetamidinate → C42H46CdN2S2Si2 + N,N'-bis(isopropyl)ethanimidamide (106500-93-0)

Guidance literature:

In toluene; at 20 ℃; for 0.5h;

DOI:10.1021/acs.inorgchem.0c03307

upstream raw materials:

isopropylamine

acetonitrile

Trimethyl orthoacetate

copper(I) N,N'-di-isopropylacetamidinate

Downstream raw materials:

copper(I) N,N'-di-isopropylacetamidinate

Refernces

• 1、 Lamb, Adam C.,Wang, Zheng,Cook, Tabitha M.,Sharma, Bhavna,Chen, Shu-Jian,Lu, Zheng,Steren, Carlos A.,Lin, Zhenyang,Xue, Zi-Ling. "Preparation of all N-coordinated zirconium amide amidinates and studies of their reactions with dioxygen and water". . p. 2 - 14. Retrieved 2016.
• 2、 -. "METAL-CONTAINING COMPOUND, PROCESS FOR PRODUCING THE SAME, METAL-CONTAINING THIN FILM, AND METHOD OF FORMING THE SAME". Page/Page column 11. . Retrieved 2010/11/25.