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Methyl 4-[(ethoxycarbonyl){[methyl(propan-2-yloxy)phosphoryl]methyl}amino]butanoate is a complex organic compound with the molecular formula C14H28NO7P. It is a derivative of a phosphonate ester, which is characterized by the presence of a phosphorus atom bonded to a carbon atom through a carbonyl group. methyl 4-[(ethoxycarbonyl){[methyl(propan-2-yloxy)phosphoryl]methyl}amino]butanoate features a butanoate chain with a 4-amino group, which is substituted by a complex side chain. The side chain includes an ethoxycarbonyl group, a methyl group, and a propan-2-yloxy group attached to a phosphoryl group. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and potentially as a precursor in the development of pharmaceuticals or agrochemicals. Its structure and properties make it a candidate for further study in various chemical and biological applications.

5577-62-8

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5577-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5577-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5577-62:
(6*5)+(5*5)+(4*7)+(3*7)+(2*6)+(1*2)=118
118 % 10 = 8
So 5577-62-8 is a valid CAS Registry Number.

5577-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-[ethoxycarbonyl-[[methyl(propan-2-yloxy)phosphoryl]methyl]amino]butanoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5577-62-8 SDS

5577-62-8Downstream Products

5577-62-8Relevant academic research and scientific papers

Transition metal-free: N -fluoroalkylation of amines using cyanurate activated fluoroalcohols

Haghighi, Fatemeh,Panahi, Farhad,Golbon Haghighi, Mohsen,Khalafi-Nezhad, Ali

supporting information, p. 12650 - 12653 (2017/12/02)

A novel and highly efficient method for N-fluoroalkylation of amines using 2,4,6-tris(fluoroalkoxy)-1,3,5-triazines was developed. This simple approach allowed the N-fluoroalkylation of amines under fast, mild and efficient reaction conditions, without using a transition metal as a catalyst.

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