84907-81-3

Basic information

• Product Name: D-Serine, O-(phenylmethyl)-, methyl ester
• Synonyms: Ser(Bn)-OMe;NH2-Ser(Bn)-OMe;(2S)-O-benzylserine methyl ester;O-benzyl-L-serine methyl ester;NH2-Ser(Bzl)-OMe
• CAS NO: 84907-81-3
• Molecular Formula: C11H15NO3
• Molecular Weight: 209.245
• Mol File: 84907-81-3.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: D-Serine, O-(phenylmethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: D-Serine, O-(phenylmethyl)-, methyl ester(84907-81-3)
• EPA Substance Registry System: D-Serine, O-(phenylmethyl)-, methyl ester(84907-81-3)

Safety Data

• Hazardous Substances Data: 84907-81-3(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 4726-96-9 O-Benzyl-L-serine 
• 10433-52-0 O-benzyl-D-serine 
• 75-77-4 chloro-trimethyl-silane 
• 47173-80-8 N-Boc-D-serine(Bzl)-OH 
• 5445-44-3 O-benzylserine 
• 3587-60-8 Benzyloxymethyl chloride 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 67389-47-3 (R)-3-benzyloxy-2-tert-butoxycarbonyl-amino-propionic acid methyl ester 
• 143730-33-0 (3R,6S)-6-benzyloxymethyl-3-isopropyl-2,5-dimethoxy-3,6-dihydropyrazine 
• 75671-91-9 Z(OMe)-Ser(Bzl)-OMe 
• 98695-13-7 (S)-methyl 3-(benzyloxy)-2-(benzyloxycarbonylamino)propanoate 
• 84907-80-2 (3S,6R)-6-Benzyloxy-2,5-dimethoxy-3-(3,4-dimethoxybenzyl)-3-methyl-3,6-dihydropyrazine 
• 80963-10-6 methyl O-benzyl-N-(tert-butoxycarbonyl)-L-serinate 

Downstream Products

• 752251-21-1 (2R)-3-benzyloxy-2-((2S)-3-benzyloxy-2-tert-butoxycarbonylamino-butyrylamino)propionic acid methyl ester 
• 158612-99-8 (4S)-4-[(benzyloxy)methyl]-1,3-oxazolidin-2-one 
• 159309-75-8 (S)-4-Benzyloxymethyl-3-(tert-butyl-dimethyl-silanyl)-oxazolidin-2-one 
• 193273-93-7 (R)-3-Benzyloxy-2-(2-tert-butoxycarbonylamino-2-methyl-propionylamino)-propionic acid methyl ester 
• 55895-93-7 methyl benzyloxy-α-diazopropionate 
• 58577-88-1 (2S)-2-amino-3-(benzyloxy)propan-1-ol 
• 1189331-41-6 (5R)-5-[(benzyloxy)methyl]-[1,3,4]-oxathiazinane-3,3-dioxide 
• 1004316-30-6 C₂₀H₂₇N₃O₄S 

Relevant articles and documents

Design, synthesis and anticancer mechanistic studies of linked azoles

Herein we report the synthesis and biological activity evaluation of 2,4 linked azole-containing molecules. A total of 13 linked thiazole- and oxazole-containing compounds were synthesized in good yields. Cytotoxicity evaluation of those compounds showed

Mechanistic studies of sanguinamide B derivatives: A unique inhibitor of eukaryotic ribosomes

Described are mechanistic studies of two Sanguinamide B (San B) derivatives. These compounds were identified as eukaryotic ribosomal inhibitors. Two biotinylated San B derivatives were synthesized and used to capture protein targets in a pull-down assay.

Synthesis of new oxathiazinane dioxides and their in vitro cancer cell growth inhibitory activity

New oxathiazinane dioxides derived from d- and l-serine have been tested for their in vitro cell growth inhibitory activity toward SKBR3 breast cancer cells. Compound (R)-24 (R′ = BrCH2C6H 4-C6H4CH2) showed a cytotoxicity with IC50 ≈ 10 μM.