Boc-L-homoserine

Modify Date: 2024-01-02 19:03:37

Boc-L-homoserine Structure
Boc-L-homoserine structure
Common Name Boc-L-homoserine
CAS Number 41088-86-2 Molecular Weight 219.235
Density 1.2±0.1 g/cm3 Boiling Point 421.6±40.0 °C at 760 mmHg
Molecular Formula C9H17NO5 Melting Point 140°C(lit.)
MSDS Chinese USA Flash Point 208.8±27.3 °C

 Use of Boc-L-homoserine


Boc-L-Homoserine is a serine derivative[1].

 Names

Name Boc-L-homoserine
Synonym More Synonyms

 Boc-L-homoserine Biological Activity

Description Boc-L-Homoserine 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 421.6±40.0 °C at 760 mmHg
Melting Point 140°C(lit.)
Molecular Formula C9H17NO5
Molecular Weight 219.235
Flash Point 208.8±27.3 °C
Exact Mass 219.110672
PSA 95.86000
LogP 0.69
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.485
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases 26-36-37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090

 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
Synthesis of the functionalizable methionine surrogate azidohomoalanine using Boc-homoserine as precursor.

Nat. Protoc. 2 , 1884-1887, (2007)

This protocol describes a synthetic route to the non-canonical amino acid azidohomoalanine (AHA) using protected homoserine as a starting material. An alternative route to AHA is presented in a compan...

 Synonyms

L-Homoserine, N-[(1,1-dimethylethoxy)carbonyl]-
N-Boc-L-Homoserine
Boc-L-Homoserine
(2S)-4-hydroxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
N-(tert-Butoxycarbonyl)-L-homoserine
(S)-2-((tert-Butoxycarbonyl)amino)-4-hydroxybutanoic acid
(S)-2-(Boc-amino)-4-hydroxybutyric Acid
Boc-Homoser-OH
N-T-Boc-L-Homoserine
Boc-Homoserine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-homoserine
(S)-2-(tert-Butoxycarbonylamino)-4-hydroxybutyric Acid
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