H-Ser(tBu)-OtBu.HCl

Names

[ Name ]:
H-Ser(tBu)-OtBu.HCl

[Synonym ]:
H-Ser(tBu)-OtBu*HCl
O-tert-Butyl-L-serine tert-butyl ester hydrochloride
O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HCL
2-Methyl-2-propanyl O-(2-methyl-2-propanyl)-L-serinate hydrochloride (1:1)
H-L-SER(TBU)-OTBU HCL
O-t-butyl-DL-serine t-butyl ester hydrochloride
O-tert-Butyl-L-serine-butyl ester hydrochloride
MFCD00034850
L-Serine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester, hydrochloride (1:1)
O-tert-Butylserine tert-butyl ester hydrochloride
Ser(tBu)-OtBu.HCl
H-SER(BUT)-OBUT HCL
L-serine tert-butyl ether tert-butyl ester hydrochloride
O-TERT-BUTYL-L-SERINE T-BUTYL ESTER HYDROCHLORIDE
tert-butyl O-(tert-butyl)-L-serinate hydrochloride
O-T-BUTYL-L-SERINE T-BUTYL ESTER HYDROCHLORIDE
DL-3-(t-Butoxy)alanine t-butyl ester hydrochloride
H-Ser(But)-ObutHCl

Biological Activity

[Description]:

H-Ser(tBu)-OtBu.HCl is a serine 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

[ Density]:
0.969g/cm3

[ Boiling Point ]:
283.8ºC at 760mmHg

[ Melting Point ]:
155 °C(dec.)

[ Molecular Formula ]:
C₁₁H₂₄ClNO₃

[ Molecular Weight ]:
253.766

[ Flash Point ]:
81.3ºC

[ Exact Mass ]:
253.144470

[ PSA ]:
61.55000

[ LogP ]:
2.97280

[ Index of Refraction ]:
1.447

[ Storage condition ]:
Store at 0-5°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

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Articles

Structure and synthesis of an immunoactive lipopeptide, WS1279, of microbial origin.

Chem. Pharm. Bull. 39 , 607, (1991)

The structure of WS1279, isolated from Streptomyces sp. as an immunoactive lipopeptide, has been deduced on the basis of chemical and physical evidence as S-[2,3-bis(palmitoyloxy)propyl]-N alpha-palmi...

Chemical synthesis and surface activity of lung surfactant phospholipid analogs. III. Chiral N-substituted ether-amide phosphonolipids.

Chem. Phys. Lipids 58 , 81, (1991)

A homologous series of chiral (R) ether-amide phosphonolipid analogs of naturally occurring (R) glycerophospholipids were synthesized and characterized for their interfacial behaviors. The phosphonoli...

H. Paulsen, K. Adermann

Liebigs Ann. Chem. , 751, (1989)

Related Compounds

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