Catalog No.:AA00A66P

122709-20-0 | tert-Butyl (s)-1-(n-methoxy-n-methylcarbamoyl)-2-hydroxyethylcarbamate

Name: Name:tert-Butyl (s)-1-(n-methoxy-n-methylcarbamoyl)-2-hydroxyethylcarbamate
Brand: AABLOCKS
SKU: AA00A66P
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250mg

97%

in stock

$45.00 $32.00

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97%

in stock

$118.00 $83.00

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97%

in stock

$319.00 $224.00

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25g

97%

in stock

$1,344.00 $941.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00A66P

Chemical Name:

tert-Butyl (s)-1-(n-methoxy-n-methylcarbamoyl)-2-hydroxyethylcarbamate

CAS Number:

122709-20-0

Molecular Formula:

C10H20N2O5

Molecular Weight:

248.2762

MDL Number:

MFCD11041264

SMILES:

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

Properties

Downstream Synthesis Route

3262-72-4

6638-79-5

122709-20-0

[1]Patent:EP2851092,2015,A1.Locationinpatent:Paragraph0088

[2]Patent:WO2015/40140,2015,A1.Locationinpatent:Page/Pagecolumn68;69

[3]OrganicandBiomolecularChemistry,2011,vol.9,p.1823-1830

[4]Patent:US2010/93720,2010,A1.Locationinpatent:Page/Pagecolumn47-48

[5]Chemistry-AnAsianJournal,2011,vol.6,p.180-188

[6]JournalofOrganicChemistry,2004,vol.69,p.3233-3235

[7]JournalofOrganicChemistry,2005,vol.70,p.10260-10270

[8]Patent:US2010/93720,2010,A1.Locationinpatent:Page/Pagecolumn36-37

[9]JournaloftheAmericanChemicalSociety,2012,vol.134,p.9291-9295

[10]JournalofOrganicChemistry,2016,vol.81,p.7373-7383

[11]OrganicandBiomolecularChemistry,2007,vol.5,p.3826-3833

[12]Synlett,2017,vol.28,p.815-818

[13]ChemicalCommunications,2014,vol.50,p.433-435

[14]JournalofMedicinalChemistry,1992,vol.35,p.3949-3955

[15]OrganicLetters,2006,vol.8,p.5569-5572

[16]Heterocycles,2006,vol.70,p.423-459

[17]AngewandteChemie-InternationalEdition,2009,vol.48,p.8124-8128

[18]TetrahedronLetters,2014,vol.55,p.6903-6906

[19]BioorganicandMedicinalChemistry,2015,vol.23,p.2989-2994

[20]Patent:US2015/238597,2015,A1.Locationinpatent:Paragraph0228

[21]AdvancedSynthesisandCatalysis,2016,vol.358,p.34-40

[22]BioorganicandMedicinalChemistry,2016,vol.24,p.3579-3595

[23]AngewandteChemie-InternationalEdition,2017,vol.56,p.2790-2794 Angew.Chem.,2017,vol.129,p.2834-2838,5

[24]Patent:WO2017/203474,2017,A1.Locationinpatent:Page/Pagecolumn24

[25]Patent:WO2008/151304,2008,A1.Locationinpatent:Page/Pagecolumn118-119

115186-34-0

122709-20-0

[1]JournaloftheChemicalSociety.PerkintransactionsI,1994,p.1275-1280

122709-20-0

77-76-9

122709-21-1

[1]TetrahedronLetters,2014,vol.55,p.6903-6906

[2]HelveticaChimicaActa,1992,vol.75,p.865-882

[3]Heterocycles,2006,vol.70,p.423-459

[4]Patent:EP2851092,2015,A1.Locationinpatent:Paragraph0088

[5]Patent:WO2015/40140,2015,A1.Locationinpatent:Page/Pagecolumn68;69

[6]Patent:US2015/238597,2015,A1.Locationinpatent:Paragraph0228

[7]Patent:WO2008/151304,2008,A1.Locationinpatent:Page/Pagecolumn118-119

3262-72-4

1117-97-1

122709-20-0

[1]HelveticaChimicaActa,1992,vol.75,p.865-882

[2]ChemicalCommunications,2014,vol.50,p.13797-13800

122709-20-0

58479-61-1

2-(tert-butyldiphenyl-silanyloxy)-1-(methoxy-methyl-carbamoyl)-ethyl-carbamicacidtert-butylester

[1]AngewandteChemie-InternationalEdition,2017,vol.56,p.2790-2794 Angew.Chem.,2017,vol.129,p.2834-2838,5

[2]OrganicandBiomolecularChemistry,2007,vol.5,p.3826-3833

[3]TetrahedronAsymmetry,2000,vol.11,p.2653-2659

Literature

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SDS