Catalog No.:AA002PNR

2488-15-5 | Boc-L-Met-OH

Name: Name:Boc-L-Met-OH
Brand: AABLOCKS
SKU: AA002PNR
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Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Upstream Synthesis Route
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA002PNR

Chemical Name:

Boc-L-Met-OH

CAS Number:

2488-15-5

Molecular Formula:

C10H19NO4S

Molecular Weight:

249.3272

MDL Number:

MFCD00065586

SMILES:

CSCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C

Properties

BP:

415.5°C at 760 mmHg

Form:

Solid

MP:

47-53 °C

Refractive Index:

-22 ° (C=1.3, AcOH)

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

250

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.6

Upstream Synthesis Route

2488-15-5

14486-03-4

[1]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1984,p.2305-2308

63-68-3

24424-99-5

2488-15-5

[1]AntimicrobialAgentsandChemotherapy,2017,vol.61,#3,

[2]TetrahedronLetters,1994,vol.35,#14,p.2121-2124

[3]Patent:EP2647624,2013,A1,.Locationinpatent:Paragraph0040;0041

[4]OrganicSyntheses,1985,vol.63,p.160-160

[5]TetrahedronLetters,2018,p.4267-4271

[6]ChemistryofNaturalCompounds,1979,vol.15,p.471-476

[7]KhimiyaPrirodnykhSoedinenii,1979,vol.15,p.543-548

[8]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,#4,p.242-249

[9]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,#4,p.250-256

[10]JournaloftheChemicalSociety-SeriesChemicalCommunications,1989,#22,p.1740-1742

[11]JournalofMedicinalChemistry,2003,vol.46,#16,p.3502-3507

[12]Bioorganicandmedicinalchemistryletters,2004,vol.14,#1,p.275-278

[13]Organicletters,2002,vol.4,#23,p.4005-4008

[14]BioorganicandMedicinalChemistry,2008,vol.16,#23,p.9984-9990

[15]BioorganicandMedicinalChemistry,2010,vol.18,#2,p.887-895

[16]JournalofEnzymeInhibitionandMedicinalChemistry,2011,vol.26,#4,p.506-513

[17]ZeitschriftfurNaturforschung-SectionBJournalofChemicalSciences,2012,vol.67,#7,p.731-746

[18]Molecules,2014,vol.19,#10,p.16349-16372

[19]Chemistry-AEuropeanJournal,2015,vol.21,#51,p.18589-18593

[20]Molecules,2016,vol.21,#2,

[21]OrganicandBiomolecularChemistry,2017,vol.15,#40,p.8493-8498

[22]Chemistry-AnAsianJournal,2018,vol.13,#4,p.400-403

63-68-3

34619-03-9

2488-15-5

[1]Patent:US2013/281695,2013,A1,.Locationinpatent:Paragraph0082-0084

63-68-3

98015-52-2

2488-15-5

[1]Synthesis,1986,#8,p.627-632

63-68-3

2488-15-5

[1]ChemistryLetters,1984,p.237-238

[2]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),1984,p.2305-2308

Downstream Synthesis Route

2488-15-5

7536-58-5

13734-34-4

47355-10-2

Boc-Gly

23446-11-9

[1]CollectionofCzechoslovakChemicalCommunications,1991,vol.56,p.2209-2217

2488-15-5

7536-58-5

13734-34-4

47355-10-2

Boc-Gly-OH,1-<3-(4-hydroxyphenyl)-1-oxopropoxy>-2,5-pyrrolidinedione

72163-37-2

[1]JournalofMedicinalChemistry,1991,vol.34,p.1125-1136

2488-15-5

7536-58-5

13734-34-4

47355-10-2

Boc-Gly-OH,1-<3-<(4-carboxymethyl)phenyl>-1-oxopropoxy>-2,5-pyrrolidinedione

127153-35-9

[1]JournalofMedicinalChemistry,1991,vol.34,p.1125-1136

2488-15-5

7536-58-5

13734-34-4

47355-10-2

Boc-Gly-OH,4-<5-(1,1-dimethylethyl)-2H-tetrazol-5-yl>benzenepropanoicacid

127153-43-9

[1]JournalofMedicinalChemistry,1991,vol.34,p.1125-1136

2488-15-5

7536-58-5

13734-34-4

47355-10-2

Boc-Gly-OH,(+/-)-α-(acetylamino)-4-<2-(1,1-dimethylethyl)-2H-tetrazol-5-yl>benzenepropanoicacid

127153-30-4

127153-31-5

[1]JournalofMedicinalChemistry,1991,vol.34,p.1125-1136

Literature

Title: Targeting of a platinum-bound sunitinib analog to renal proximal tubular cells.

Journal: International journal of nanomedicine 20120101

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

Title: Cooperation between aspirin-triggered lipoxin and nitric oxide (NO) mediates antiadhesive properties of 2-(Acetyloxy)benzoic acid 3-(nitrooxymethyl)phenyl ester (NCX-4016) (NO-aspirin) on neutrophil-endothelial cell adherence.

Journal: The Journal of pharmacology and experimental therapeutics 20040601

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