Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: (S)-METHYL 2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)AMINO)-3-HYDROXYPROPANOATE
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Purity: 98.0%
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82911-78-2

82911-78-2 structure

Name: Fmoc-ser-ome
Chemical Name: (S)-Methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxypropanoate
CAS Number: 82911-78-2
Molecular Formula: C₁₉H₁₉NO₅
Molecular Weight: 341.358
Catalog: Biochemical Amino acids and their derivatives Serine derivative
Create Date: 2018-04-14 08:00:00
Modify Date: 2025-08-26 10:27:23
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].

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

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 >> Others Signaling 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.

HS Code	2924299090

5680-80-8

82911-69-1

~98%

82911-78-2

Literature: Shao, Hui; Lockman, Jeffrey W.; Parquette, Jon R. Journal of the American Chemical Society, 2007 , vol. 129, # 7 p. 1884 - 1885

73724-45-5

74-88-4

~94%

82911-78-2

Literature: Zhang, Fa; Zhang, Wei; Zhang, Yan; Curran, Dennis P.; Liu, Gang Journal of Organic Chemistry, 2009 , vol. 74, # 6 p. 2594 - 2597

186581-53-3

73724-45-5

82911-78-2

Literature: Bioorganic and Medicinal Chemistry, , vol. 22, # 4 p. 1421 - 1428

2788-84-3

82911-69-1

~80%

82911-78-2

Literature: Lapatsanis, Lucas; Milias, George; Froussios, Kleanthis; Kolovos, Miltiadis Synthesis, 1983 , # 8 p. 671 - 673

67-56-1

73724-45-5

82911-78-2

Literature: Organic letters, , vol. 3, # 16 p. 2477 - 2479

24324-17-2

82911-78-2

Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980

82911-72-6

82911-78-2

Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980

101-83-7

82911-78-2

Literature: Canadian Journal of Chemistry, , vol. 60, p. 976 - 980

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%