91177-57-0

Basic information

• Product Name: BOC-D-METHIONINOL
• Synonyms: BOC-(R)-2-AMINO-4-METHYLTHIO-1-BUTANOL;BOC-D-MET-OL;BOC-D-METHIONINOL;N-ALPHA-T-BOC-D-METHIONINOL;N-BOC-D-METHIONINOL;N-T-BUTOXYCARBONYL-D-METHIONINOL;NALPHA-tert-Butoxycarbonyl-D-methioninol;(R)-2-t-Butyloxycarbonyl-amino-4-methylthio-1-butanol, N-alpha-t-Butyloxycarbonyl-D-methioninol
• CAS NO: 91177-57-0
• Molecular Formula: C₁₀H₂₁NO₃S
• Molecular Weight: 235.34
• Product Categories: Amino Acids
• Mol File: 91177-57-0.mol
• Article Data: 6

Chemical Properties

• Appearance: Colorless crystalline
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: BOC-D-METHIONINOL(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-D-METHIONINOL(91177-57-0)
• EPA Substance Registry System: BOC-D-METHIONINOL(91177-57-0)

Safety Data

• Hazardous Substances Data: 91177-57-0(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 5241-66-7 (R)-N-(tert-butoxycarbonyl)methionine 
• 348-67-4 D-methionine 
• 34619-03-9 tert-butyldicarbonate 
• 502-83-0 (R)-2-amino-4-methylthio-1-butanol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 2488-15-5 N-t-butoxycarbonyl-D-methionine 
• 33900-24-2 (R)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyric acid methyl ester 

Downstream Products

• 502-83-0 (R)-2-amino-4-methylthio-1-butanol 
• 300363-41-1 (+)-1,1-dimethylethyl [(1R)-1-({[(1,1-dimethylethyl)(diphenyl)silyl]oxy}methyl)prop-2-en-1-yl]carbamate 
• 89985-86-4 (R)-2-(N-tert-butoxycarbonylamino)-3-buten-1-ol 
• 91103-44-5 (S)-2-(tert-Butoxycarbonyl-{(R)-2-[tert-butoxycarbonyl-((R)-2-tert-butoxycarbonylamino-3-hydroxy-propyl)-amino]-3-hydroxy-propyl}-amino)-succinic acid dibenzyl ester 
• 91103-43-4 (S)-2-{(R)-2-[tert-Butoxycarbonyl-((R)-2-tert-butoxycarbonylamino-3-hydroxy-propyl)-amino]-3-hydroxy-propylamino}-succinic acid dibenzyl ester 
• 91103-39-8 3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (R)-4-methylsulfanyl-2-(3,3,3-trifluoro-2-methoxy-2-phenyl-propionylamino)-butyl ester 
• 91103-36-5 N-tert.-butyloxycarbonyl-L-serinal 

Relevant articles and documents

Design, synthesis and biological evaluation of isoxazole-based CK1 inhibitors modified with chiral pyrrolidine scaffolds

In this study, we report on the modification of a 3,4-diaryl-isoxazole-based CK1 inhibitor with chiral pyrrolidine scaffolds to develop potent and selective CK1 inhibitors. The pharmacophore of the lead structure was extended towards the ribose pocket of

3-Amino-2-hydroxyamides and related compounds as inhibitors of methionine aminopeptidase-2

Substituted 3-amino-2-hydroxyamides and related hydroxyamides and acylhydrazines were identified as inhibitors of human methionine aminopeptidase-2 (MetAP2). Examination of substituents through parallel synthesis and iterative structure-based design allow

3-Amino-2-hydroxyalkanoic acids and their prodrugs

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