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N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 163769-72-0 Structure
  • Basic information

    1. Product Name: N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE
    2. Synonyms: N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE
    3. CAS NO:163769-72-0
    4. Molecular Formula: C6H11Cl3N2O2
    5. Molecular Weight: 249.52274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163769-72-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE(163769-72-0)
    11. EPA Substance Registry System: N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE(163769-72-0)
  • 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: 163769-72-0(Hazardous Substances Data)

163769-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163769-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,7,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 163769-72:
(8*1)+(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*7)+(1*2)=170
170 % 10 = 0
So 163769-72-0 is a valid CAS Registry Number.

163769-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trichloro-N'-(2,2-dimethoxyethyl)ethanimidamide

1.2 Other means of identification

Product number -
Other names N-(2,2-DIMETHOXYETHYL)TRICHLOROACETAMIDINE

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:163769-72-0 SDS

163769-72-0Downstream Products

163769-72-0Relevant articles and documents

New blue phosphorescent heteroleptic Ir(iii) complexes with imidazole- and: N -methylimidazole carboxylates as ancillary ligands

Chae, Eun Ah,Chung, Won Jae,Hwang, Do-Hoon,Jang, Jae-Ho,Lee, Jun Yeob,Park, Hea Jung,Seo, Hye Won,Yoon, Ung Chan

, p. 13843 - 13851 (2020/11/04)

Imidazole- and N-methylimidazole carboxylate have been introduced to serve as ancillary ligands in heteroleptic Ir(iii) complexes containing 2-phenylpyridine-based main ligands, with consideration of the frontier orbital energy levels. Complexes Ir1-Ir4 were synthesized and found to have LUMO levels higher than that of the corresponding Ir(iii) complex containing pyridyl carboxylate. All the synthesized Ir(iii) complexes exhibited blue phosphorescence emission maxima in the region of 465-467 nm at room temperature. Phosphorescent quantum efficiencies were increased by a factor of 1.8-6.7 by blocking the intermolecular hydrogen bonding between the imidazole carboxylate ligands of neighboring Ir(iii) complexes, which was achieved by N-methylation of the imidazole carboxylate ancillary ligand. The organic light-emitting diodes fabricated using Ir3 and Ir4 as dopant materials in the emissive layers were found to emit blue emission with peaks at 469 and 471 nm and maximum external quantum efficiencies of 20.0 and 22.4%, respectively. Moreover, all the fabricated devices with Ir3 and Ir4 exhibited low efficiency roll-off, indicating excellent stability of the materials.

Novel synthesis of heterocyclic aryl amidines

Tommasi, Ruben A.,Macchia, William M.,Parker, David T.

, p. 5947 - 5950 (2007/10/03)

We have developed a novel amidine synthesis that allows the preparation of heterocyclic amidines that were previously unknown and difficult to prepare by published methods. The route involves the lithiation of heterocycles by the action of n-BuLi followed

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