CAS 82911-78-2|Fmoc-ser-ome

Introduction：Basic information about CAS 82911-78-2|Fmoc-ser-ome, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Fmoc-ser-ome BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Synonyms

Common Name	Fmoc-ser-ome
CAS Number	82911-78-2	Molecular Weight	341.358
Density	1.3±0.1 g/cm3	Boiling Point	579.4±45.0 °C at 760 mmHg
Molecular Formula	C₁₉H₁₉NO₅	Melting Point	/
MSDS	/	Flash Point	304.2±28.7 °C

Names

Name	(S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxypropanoate
Synonym	More Synonyms

Fmoc-ser-ome BiologicalActivity

Description	Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor[1][2].
Related Catalog	Research Areas >>OthersSignaling Pathways >>Others >>Others
References	[1]. Tamiaki H, et al. Synthesis of chlorophyll-amino acid conjugates as models for modification of proteins with chromo/fluorophores. Bioorg Med Chem. 2014 Feb 15;22(4):1421-8. [2]. Kärkkäinen TS, et al. Iodine-mediated glycosylation en route to mucin-related glyco-aminoacids and glycopeptides. Carbohydr Res. 2008 Jul 21;343(10-11):1830-4.

Description

Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor[1][2].

Related Catalog

Research Areas >>OthersSignaling Pathways >>Others >>Others

References

[1]. Tamiaki H, et al. Synthesis of chlorophyll-amino acid conjugates as models for modification of proteins with chromo/fluorophores. Bioorg Med Chem. 2014 Feb 15;22(4):1421-8.

[2]. Kärkkäinen TS, et al. Iodine-mediated glycosylation en route to mucin-related glyco-aminoacids and glycopeptides. Carbohydr Res. 2008 Jul 21;343(10-11):1830-4.

Chemical & Physical Properties

Density	1.3±0.1 g/cm3
Boiling Point	579.4±45.0 °C at 760 mmHg
Molecular Formula	C₁₉H₁₉NO₅
Molecular Weight	341.358
Flash Point	304.2±28.7 °C
Exact Mass	341.126312
PSA	88.35000
LogP	3.25
Vapour Pressure	0.0±1.7 mmHg at 25°C
Index of Refraction	1.595
InChIKey	QQQVLIVWQMWACQ-KRWDZBQOSA-N
SMILES	COC(=O)C(CO)NC(=O)OCC1c2ccccc2-c2ccccc21
Storage condition	-15°C

Safety Information

HS Code	2924299090

Customs

HS Code	2924299090
Summary	2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Synonyms

Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, methyl ester

Methyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]serinate

methyl (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoate

Fmoc-Ser-Ome

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