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Diethyl (acetylamino)(hexyl)propanedioate is a complex organic compound with the chemical formula C19H35NO5. It is a derivative of propanedioic acid, featuring a hexyl chain and an acetylamino group attached to the central carbon atom. diethyl (acetylamino)(hexyl)propanedioate is characterized by its ester and amide functional groups, which contribute to its chemical properties. It is synthesized through a series of chemical reactions involving the combination of diethyl propanedioate with an acetylamino group. Due to its unique structure, diethyl (acetylamino)(hexyl)propanedioate has potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, where it can serve as an intermediate in the synthesis of more complex molecules or as a component in formulations. Its specific use and properties depend on the context in which it is applied, and further research may be required to fully understand its potential and limitations.

5463-91-2

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5463-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5463-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5463-91:
(6*5)+(5*4)+(4*6)+(3*3)+(2*9)+(1*1)=102
102 % 10 = 2
So 5463-91-2 is a valid CAS Registry Number.

5463-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-acetamido-2-hexylpropanedioate

1.2 Other means of identification

Product number -
Other names acetylamino-hexyl-malonic acid diethyl ester

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:5463-91-2 SDS

5463-91-2Downstream Products

5463-91-2Relevant academic research and scientific papers

Pro-apoptotic activity of lipidic α-amino acids isolated from Protopalythoa variabilis

Wilke, Diego Veras,Jimenez, Paula Christine,Araújo, Renata Mendona,Da Silva, Wildson Max Barbosa,Pessoa, Otília Deusdênia Loiola,Silveira, Edilberto Rocha,Pessoa, Claudia,De Moraes, Manoel Odorico,Skwarczynski, Mariusz,Simerska, Pavla,Toth, Istvan,Costa-Lotufo, Letícia Veras

scheme or table, p. 7997 - 8004 (2011/02/23)

Lipidic α-amino acids (LAAs) have been described as non-natural amino acids with long saturated or unsaturated aliphatic chains. In the continuing prospect to discover anticancer agents from marine sources, we have obtained a mixture of two cytotoxic LAAs (1a and 1b) from the zoanthid Protopalythoa variabilis. The anti-proliferative potential of 14 synthetic LAAs and 1a/1b were evaluated on four tumor cell lines (HCT-8, SF-295, MDA-MB-435, and HL-60). Five of the synthetic LAAs showed high percentage of tumor cell inhibition, while 1a/1b completely inhibited tumor cell growth. Additionally, apoptotic effects of 1a/1b were studied on HL-60 cell line. 1a/1b-treated cells showed apoptosis morphology, loss of mitochondrial potential, and DNA fragmentation.

Microwave-assisted synthesis of unnatural amino acids

Young, Douglas D.,Torres-Kolbus, Jessica,Deiters, Alexander

experimental part, p. 5478 - 5480 (2009/05/30)

Microwave irradiation has been proven to be a useful tool in the rapid assembly of racemic unnatural amino acids in only two steps. Additional benefits of this methodology are the commercial availability of the inexpensive starting materials and the high yields and high purities of the final amino acid products.

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