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5721-12-0

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5721-12-0 Usage

General Description

ETHYL 2,6-DIAMINOHEXANOATE DIHYDROCHLORIDE, also known as ethyl hexanedioate dihydrochloride, is a chemical compound with the molecular formula C8H20Cl2N2O2. It is a dihydrochloride salt of ethyl 2,6-diaminohexanoate, and it is commonly used as a pharmaceutical intermediate in the synthesis of various drugs and pharmaceutical compounds. ETHYL 2,6-DIAMINOHEXANOATE DIHYDROCHLORIDE is a white to off-white crystalline powder that is soluble in water and alcohol. It is a derivative of ethylhexanoic acid and is used in the production of various drugs, such as statins and other cardiovascular medications. It is also used in the production of chiral compounds and as a building block in the synthesis of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 5721-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5721-12:
(6*5)+(5*7)+(4*2)+(3*1)+(2*1)+(1*2)=80
80 % 10 = 0
So 5721-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2O2.2ClH/c1-2-12-8(11)7(10)5-3-4-6-9;;/h7H,2-6,9-10H2,1H3;2*1H

5721-12-0SDS

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 ethyl 2,6-diaminohexanoate,dihydrochloride

1.2 Other means of identification

Product number -
Other names Ethyl DL-lysinate HCl

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:5721-12-0 SDS

5721-12-0Relevant articles and documents

Interfacial synthesis and properties of l-lysine-derived optically active poly(ester-imide)s

Zahmatkesh, Saeed,Alborzi, Ali Reza,Sadeghi, Javad,Zare, Karim

scheme or table, p. 607 - 610 (2012/02/01)

l-Lysine hydrochloride was transformed to ethyl l-lysine dihydrochloride. This salt was reacted with trimellitic anhydride to yield the corresponding diacid (1). Interfacial polycondensation results novel poly(ester-imide)s (PEIa-i). These polymers have inherent viscosities in the range of 0.23-0.47 dl g-1, display optical activity, and are readily soluble in polar aprotic solvents. They start to decompose (T10%) above 350 °C and display glass-transition temperatures at 100.42-172.81 °C. All of the above polymers were fully characterized by UV, FT-IR and 1H NMR spectroscopy, elemental analysis, TGA, DSC, inherent viscosity measurement and specific rotation.

Synthesis and antimicrobial characterization of novel l-lysine gemini surfactants pended with reactive groups

Tan, Hong,Xiao, Huining

, p. 1759 - 1761 (2008/09/18)

A series of novel quaternary ammonium gemini surfactants of l-lysine containing ester group were synthesized with high yield rate. The antibacterial and antifungal activities of these gemini surfactants were evaluated by quantifying the minimal inhibitory concentration (MIC). The results indicated that the quaternary ammonium gemini surfactants exhibited improved activity against a broad spectrum of Gram-positive and Gram-negative bacteria as well as fungi. The pended ester group provides a reactive site for incorporating the surfactant into polymers, thus leading to the polymers with high antimicrobial efficiency.

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