Boc-Ser-OH

Modify Date: 2024-01-02 16:10:59

Boc-Ser-OH Structure
Boc-Ser-OH structure
 Common Name Boc-Ser-OH
CAS Number 3262-72-4 Molecular Weight 205.208
Density 1.2±0.1 g/cm3 Boiling Point 385.1±37.0 °C at 760 mmHg
Molecular Formula C8H15NO5 Melting Point 91 °C (dec.)(lit.)
MSDS Chinese USA Flash Point 186.7±26.5 °C

 Use of Boc-Ser-OH


(S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid is a serine derivative[1].

 Names

Name BOC-L-Serine
Synonym More Synonyms

 Boc-Ser-OH Biological Activity

Description (S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid 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 1.2±0.1 g/cm3
Boiling Point 385.1±37.0 °C at 760 mmHg
Melting Point 91 °C (dec.)(lit.)
Molecular Formula C8H15NO5
Molecular Weight 205.208
Flash Point 186.7±26.5 °C
Exact Mass 205.095016
PSA 95.86000
LogP 0.22
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.486
Storage condition 2~8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Risk Phrases R20/21/22
Safety Phrases 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%

 Articles8

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Unraveling the interplay of backbone rigidity and electron rich side-chains on electron transfer in peptides: the realization of tunable molecular wires.

J. Am. Chem. Soc. 136(35) , 12479-88, (2014)

Electrochemical studies are reported on a series of peptides constrained into either a 310-helix (1-6) or β-strand (7-9) conformation, with variable numbers of electron rich alkene containing side cha...

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...

In situ fabrication of cleavable peptide arrays on polydimethylsiloxane and applications for kinase activity assays.

Anal. Chim. Acta 865 , 53-9, (2015)

Polydimethylsiloxane (PDMS) is widely used for microfabrication and bioanalysis; however, its surface functionalization is limited due to the lack of active functional groups and incompatibility with ...

 Synonyms

Boc-L-serine
L-Serine-d3-N-t-BOC
(S)-2-(tert-Butoxycarbonylamino)-3-hydroxypropanoic acid
BOC-L-SERINE extrapure
t-butyloxycarbonyl-L-serine
N-Boc-L-serine
MFCD00037243
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-serine
L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-
BOC-L-PROLINOL LIQUID
Boc-Ser-OH
BOC-SERINE-OH
EINECS 221-867-3
BOC-L-SER-OH
(S)-2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid
BOC-L-SER
N-(tert-Butoxycarbonyl)-L-serine,Boc-L-serine
BOC-SERINE
N-(tert-Butoxycarbonyl)-L-serine
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