Catalog No.:AA003C8W

108149-63-9 | (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

Name: Name:(R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
Brand: AABLOCKS
SKU: AA003C8W
Availability: InStock
Rating: 90 (10 reviews)

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100mg

97%

in stock

$21.00 $15.00

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250mg

97%

in stock

$35.00 $25.00

- +

97%

in stock

$58.00 $41.00

- +

97%

in stock

$214.00 $150.00

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25g

96%

in stock

$976.00 $683.00

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100g

96%

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$2,804.00 $1,963.00

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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:

AA003C8W

Chemical Name:

(R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

CAS Number:

108149-63-9

Molecular Formula:

C11H21NO4

Molecular Weight:

231.2887

MDL Number:

MFCD06202686

SMILES:

OC[C@@H]1COC(N1C(=O)OC(C)(C)C)(C)C

Properties

BP:

314.07°C at 760 mmHg

Form:

Solid

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

270

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.8

Upstream Synthesis Route

95715-86-9

108149-63-9

[1]Patent:WO2005/87700,2005,A2,.Locationinpatent:Page/Pagecolumn322

[2]BioorganicandMedicinalChemistryLetters,2008,vol.18,#6,p.2067-2072

[3]OrganicSyntheses,2000,vol.77,p.64-64

[4]Patent:CN105636956,2016,A,.Locationinpatent:Paragraph0240;0241

[5]Patent:WO2009/53277,2009,A1,.Locationinpatent:Page/Pagecolumn93-94

[6]Patent:WO2008/107365,2008,A1,.Locationinpatent:Page/Pagecolumn56

[7]SyntheticCommunications,1994,vol.24,#15,p.2147-2152

[8]SyntheticCommunications,2005,vol.35,#11,p.1481-1492

[9]Chemistry-AEuropeanJournal,2017,vol.23,#30,p.7207-7211

[10]BioorganicandMedicinalChemistry,2007,vol.15,#2,p.663-677

[11]Patent:WO2005/41899,2005,A2,.Locationinpatent:Page/Pagecolumn130-132

[12]Patent:WO2005/41899,2005,A2,.Locationinpatent:Page/Pagecolumn130-132

[13]OrganicLetters,2003,vol.5,#23,p.4253-4256

[14]JournalofOrganicChemistry,2007,vol.72,#4,p.1218-1225

[15]OrganicLetters,2018,vol.20,#12,p.3574-3578

[16]Chemistry-AEuropeanJournal,2009,vol.15,#17,p.4428-4436

[17]JournaloftheBrazilianChemicalSociety,2010,vol.21,#4,p.680-685

[18]TetrahedronLetters,1989,vol.30,#29,p.3799-3802

[19]Tetrahedron,1996,vol.52,#36,p.11673-11694

[20]Synthesis,1997,#5,p.527-529

[21]JournalofOrganicChemistry,1998,vol.63,#15,p.5262-5264

[22]JournaloftheAmericanChemicalSociety,1998,vol.120,#36,p.9180-9187

[23]JournalofOrganicChemistry,2003,vol.68,#7,p.2979-2982

[24]JournalofOrganicChemistry,1987,vol.52,#12,p.2361-2364

[25]MedicinalChemistry,2014,vol.10,#6,p.609-618

[26]BioorganicandMedicinalChemistry,2015,vol.23,#4,p.759-769

[27]Patent:KR2015/31544,2015,A,.Locationinpatent:Paragraph0075-0084

[28]AngewandteChemie-InternationalEdition,2018,vol.57,#18,p.5147-5150

[29]Angew.Chem.,2018,vol.130,p.5241-5244,4

108149-60-6

108149-63-9

[1]Patent:US2016/200709,2016,A1,.Locationinpatent:Paragraph0202

[2]LifeSciences,2011,vol.89,#21-22,p.786-794

[3]OrganicandBiomolecularChemistry,2014,vol.12,#23,p.4021-4030

102308-32-7

108149-63-9

[1]JournalofOrganicChemistry,1987,vol.52,#12,p.2361-2364

[2]Synthesis,1997,#5,p.527-529

[3]OrganicSyntheses,2000,vol.77,p.64-64

[4]ChemicalCommunications,1999,#16,p.1599-1600

[5]EuropeanJournalofOrganicChemistry,2002,#7,p.1323-1336

2766-43-0

108149-63-9

[1]JournalofOrganicChemistry,2007,vol.72,#4,p.1218-1225

[2]BioorganicandMedicinalChemistry,2007,vol.15,#2,p.663-677

[3]OrganicLetters,2003,vol.5,#23,p.4253-4256

[4]Tetrahedron,1996,vol.52,#36,p.11673-11694

[5]JournalofOrganicChemistry,1987,vol.52,#12,p.2361-2364

[6]TetrahedronLetters,1989,vol.30,#29,p.3799-3802

[7]MedicinalChemistry,2014,vol.10,#6,p.609-618

[8]Patent:KR2015/31544,2015,A,

[9]OrganicSyntheses,2000,vol.77,p.64-64

[10]AngewandteChemie-InternationalEdition,2018,vol.57,#18,p.5147-5150

[11]Angew.Chem.,2018,vol.130,p.5241-5244,4

[12]OrganicLetters,2018,vol.20,#12,p.3574-3578

[13]Patent:WO2008/107365,2008,A1,

[14]Patent:WO2005/41899,2005,A2,

24424-99-5

108149-63-9

[1]OrganicLetters,2003,vol.5,#23,p.4253-4256

[2]Tetrahedron,1996,vol.52,#36,p.11673-11694

[3]JournalofOrganicChemistry,1987,vol.52,#12,p.2361-2364

[4]MedicinalChemistry,2014,vol.10,#6,p.609-618

[5]OrganicLetters,2018,vol.20,#12,p.3574-3578

Downstream Synthesis Route

693-03-8

108149-63-9

4-(1-hydroxy-pentyl)-2,2-dimethyl-oxazolidine-3-carboxylicacid<i>tert</i>-butylester

[1]TetrahedronLetters,2005,vol.46,p.8567-8571

1826-67-1

108149-63-9

256650-51-8

[1]TetrahedronLetters,2005,vol.46,p.8567-8571

108149-63-9

107-30-2

(S)-4-methoxymethoxymethyl-2,2-dimethyloxazolidine-3-carboxylicacidtert-butylester

[1]JournalofOrganicChemistry,2005,vol.70,p.4514-4516

108149-63-9

75-36-5

(S)-4-acetoxymethyl-2,2-dimethyloxazolidine-3-carboxylicacidtert-butylester

[1]JournalofOrganicChemistry,2005,vol.70,p.4514-4516

108149-63-9

58479-61-1

852609-51-9

[1]JournalofOrganicChemistry,2005,vol.70,p.4514-4516

[2]TetrahedronLetters,2007,vol.48,p.3511-3515

Literature

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SDS