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Methanaminium, N-methyl-N-(phenylmethylene)-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59836-47-4

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59836-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59836-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,3 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59836-47:
(7*5)+(6*9)+(5*8)+(4*3)+(3*6)+(2*4)+(1*7)=174
174 % 10 = 4
So 59836-47-4 is a valid CAS Registry Number.

59836-47-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzylidene(dimethyl)azanium,iodide

1.2 Other means of identification

Product number -
Other names Methanaminium,N-methyl-N-(phenylmethylene)-,iodide

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:59836-47-4 SDS

59836-47-4Relevant academic research and scientific papers

A Simple and Highly Diastereoselective One-Pot Synthesis of Mannich-Bases

Arend, Michael,Risch, Nikolaus

, p. 974 - 976 (2007/10/03)

A convenient one-pot procedure for the synthesis of β-amino ketones 5 from economical shelf reagents is described. Iminium salts 3 are generated in virtually quantitative yields from secondary amines 1 and aldehydes 2 mediated by NaI/Me3SiCl/NEt3. Subsequently, the salts 3 are used for the in situ aminoalkylation of enamines 4. The method provides the Mannich bases 5 in high yields and excellent diastereoselectivities (>96 % ds). It can also be applied for the aminoalkylation of other nucleophiles such as imines or electron-rich aromatic compounds.

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