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

Modify Date: 2024-01-08 16:26:09

Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride Structure
Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride structure
Common Name Ethyl 2-((2-((tert-butoxycarbonyl)amino)ethyl)amino)acetate hydrochloride
CAS Number 347890-34-0 Molecular Weight 282.764
Density N/A Boiling Point 352ºC at 760mmHg
Molecular Formula C11H23ClN2O4 Melting Point N/A
MSDS USA Flash Point 166.7ºC

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


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

 Names

Name ethyl 2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]acetate,hydrochloride
Synonym More Synonyms

  Biological Activity

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

 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

 Synonyms

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
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