Boc-Ser-OMe

Modify Date: 2024-01-02 01:18:51

Boc-Ser-OMe Structure
Boc-Ser-OMe structure
Common Name Boc-Ser-OMe
CAS Number 2766-43-0 Molecular Weight 219.235
Density 1.1±0.1 g/cm3 Boiling Point 354.3±32.0 °C at 760 mmHg
Molecular Formula C9H17NO5 Melting Point 42 °C
MSDS USA Flash Point 168.1±25.1 °C

 Use of Boc-Ser-OMe


Boc-Ser-OMe is a serine derivative[1].

 Names

Name methyl (2S)-3-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
Synonym More Synonyms

 Boc-Ser-OMe Biological Activity

Description Boc-Ser-OMe is a serine 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

Density 1.1±0.1 g/cm3
Boiling Point 354.3±32.0 °C at 760 mmHg
Melting Point 42 °C
Molecular Formula C9H17NO5
Molecular Weight 219.235
Flash Point 168.1±25.1 °C
Exact Mass 219.110672
PSA 84.86000
LogP 0.80
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.461

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)
Hazard Codes Xi
Safety Phrases S23-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 Synthetic Route

 Customs

HS Code 2924199090
Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles1

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

 Synonyms

Methyl N-(tert-butoxycarbonyl)-L-serinate
L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester
N-(tert-Butoxycarbonyl)-L-serine methyl ester
Boc-Ser-OMe; Boc-L-serine methyl ester
N-(Boc)-L-serine methylester
N-Boc-L-serine Methyl Ester
BOC-L-Serine methyl ester
N-(tert-Butoxycarbonyl)-L-serine methyl ester,Boc-L-serine methyl ester
(S)-Boc-serine methyl ester
Methyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-serinate
N-t-butoxycarbonyl-D,L-serine methyl ester
MFCD00191869
N-(t-butoxycarbonyl)-L-serine methyl ester
Boc-Ser-OMe
N-Boc-(S)-serine methyl ester
(N-tertbutoxycarbonyl)serine methyl ester
methyl N-t-butoxycarbonyl-D,L-serinate
N-(Boc)-L-serine methyl ester
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