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N-(4-methylbenzyl)-N-(1-phenylethyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 202199-08-4 Structure
  • Basic information

    1. Product Name: N-(4-methylbenzyl)-N-(1-phenylethyl)amine
    2. Synonyms: N-(4-methylbenzyl)-N-(1-phenylethyl)amine;AKOS JY2033517;UKRORGSYN-BB BBV-118344;(4-methylbenzyl)(1-phenylethyl)amine(SALTDATA: HCl);N-[(4-methylphenyl)methyl]-1-phenylethanamine
    3. CAS NO:202199-08-4
    4. Molecular Formula: C16H19N
    5. Molecular Weight: 225.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 202199-08-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 327.8°C at 760 mmHg
    3. Flash Point: 147.9°C
    4. Appearance: /
    5. Density: 1g/cm3
    6. Vapor Pressure: 0.000198mmHg at 25°C
    7. Refractive Index: 1.564
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(4-methylbenzyl)-N-(1-phenylethyl)amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(4-methylbenzyl)-N-(1-phenylethyl)amine(202199-08-4)
    12. EPA Substance Registry System: N-(4-methylbenzyl)-N-(1-phenylethyl)amine(202199-08-4)
  • 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: 202199-08-4(Hazardous Substances Data)

202199-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 202199-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,9 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 202199-08:
(8*2)+(7*0)+(6*2)+(5*1)+(4*9)+(3*9)+(2*0)+(1*8)=104
104 % 10 = 4
So 202199-08-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H19N/c1-13-8-10-15(11-9-13)12-17-14(2)16-6-4-3-5-7-16/h3-11,14,17H,12H2,1-2H3

202199-08-4Downstream Products

202199-08-4Relevant articles and documents

Chiral cyclometalated iridium complexes for asymmetric reduction reactions

Smith, Jennifer,Kacmaz, Aysecik,Wang, Chao,Villa-Marcos, Barbara,Xiao, Jianliang

supporting information, p. 279 - 284 (2021/01/18)

A series of chiral cyclometalated iridium complexes have been synthesised by cyclometalating chiral 2-aryl-oxazoline and imidazoline ligands with [Cp?IrCl2]2. These iridacycles were studied for asymmetric transfer hydrogenation reactions with formic acid as the hydrogen source and were found to display various activities and enantioselectivities, with the most effective ones affording up to 63% ee in the asymmetric reductive amination of ketones and 77% ee in the reduction of pyridinium ions. This journal is

Hydrogen-free reductive amination using iron pentacarbonyl as a reducing agent

Afanasyev, Oleg I.,Usanov, Dmitry L.,Chusov, Denis

supporting information, p. 10164 - 10166 (2017/12/26)

We developed solvent-free reductive amination without an external hydrogen source using iron pentacarbonyl as a reducing agent. Neither a catalyst nor any other additives were employed. Various types of substrates are suitable for the reaction, including

Graphene-supported NiPd alloy nanoparticles: A novel and highly efficient heterogeneous catalyst system for the reductive amination of aldehydes

Ni?anci, Bilal,Ganjehyan, Khadijeh,Metin, ?nder,Da?tan, Arif,T?r?k, Béla

, p. 191 - 197 (2015/09/22)

A novel and highly efficient heterogeneous catalytic reductive amination of aldehydes is described. The recently developed graphene supported NiPd alloy nanoparticle (G-NiPd) catalyst using ammonia borane (AB) as a green, stable and safe hydrogen donor was used in a water/methanol mixture (v/v = 2/3) under ambient conditions. The catalytic system was successfully applied in the reductive amination of various substituted aldehydes with amines and the corresponding products were obtained in (up to) 99% yield in 6 h. The G-NiPd catalyst could be recycled up to five times without any significant loss in the product yield.

Iridium-catalysed amine alkylation with alcohols in water

Saidi, Ourida,Blacker, A. John,Farah, Mohamed M.,Marsden, Stephen P.,Williams, Jonathan M. J.

supporting information; experimental part, p. 1541 - 1543 (2010/06/12)

Amines have been directly alkylated with alcohols using 1 mol% [Cp*IrI2]2 catalyst in water in the absence of base or other additives. The Royal Society of Chemistry 2010.

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