Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride

Names

[ Name ]:
Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride

[Synonym ]:
Ethyl N-[2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)ethyl]glycinate hydrochloride (1:1)
Glycine, N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-, ethyl ester, hydrochloride (1:1)
N-(Boc-aminoethyl)-Gly-OEt hydrochloride
Ethyl [2-(Boc-amino)ethylamino]acetate hydrochloride
ethyl n-[(2-boc-amino)ethyl]glycinatehydrochloride
Ethyl N-{2-[(tert-butoxycarbonyl)amino]ethyl}glycinate hydrochloride (1:1)
Ethyl N-[(2-Boc-amino)ethyl]glycinate HCl
N-[2-(Boc-amino)ethyl]glycine ethylester hydrochloride
h-(boc-aeg)-oet hcl
Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride

Biological Activity

[Description]:

Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

[ Boiling Point ]:
352ºC at 760mmHg

[ Molecular Formula ]:
C₁₁H₂₃ClN₂O₄

[ Molecular Weight ]:
282.764

[ Flash Point ]:
166.7ºC

[ Exact Mass ]:
282.134644

[ PSA ]:
76.66000

[ LogP ]:
2.24760

[ Storage condition ]:
?20°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

Related Compounds

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