Catalog No.:AA0032UF

92420-89-8 | 2,3,4-Tri-o-acetyl-alpha-d-glucuronic acid methyl ester, trichloroacetimidate

Name: Name:2,3,4-Tri-o-acetyl-alpha-d-glucuronic acid methyl ester, trichloroacetimidate
Brand: AABLOCKS
SKU: AA0032UF
Availability: InStock
Rating: 90 (10 reviews)

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100mg

95%

in stock

$13.00 $9.00

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250mg

95%

in stock

$16.00 $11.00

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98%

in stock

$49.00 $34.00

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98%

in stock

$137.00 $96.00

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25g

95%

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$596.00 $417.00

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100g

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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:

AA0032UF

Chemical Name:

2,3,4-Tri-o-acetyl-alpha-d-glucuronic acid methyl ester, trichloroacetimidate

CAS Number:

92420-89-8

Molecular Formula:

C15H18Cl3NO10

Molecular Weight:

478.6631

MDL Number:

MFCD02094293

SMILES:

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

Properties

BP:

442.115°C at 760 mmHg

Form:

Solid

MP:

103-105°C

Storage:

Inert atmosphere;-20 ℃;

Computed Properties

Complexity:

680

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.7

Upstream Synthesis Route

72692-06-9

545-06-2

92420-89-8

[1]CarbohydrateResearch,2003,vol.338,#22,p.2337-2340

[2]MedChemComm,2014,vol.5,#7,p.984-988

[3]JournalofChemicalResearch-PartS,1997,#10,p.370-371

[4]CarbohydrateResearch,2012,vol.349,p.108-112

[5]JournalofChemicalCrystallography,2013,vol.43,#3,p.138-143

[6]Steroids,2009,vol.74,#2,p.250-255

[7]JournalofOrganicChemistry,1984,vol.49,#25,p.4988-4993

[8]JournalofOrganicChemistry,2004,vol.69,#26,p.9159-9170

[9]TetrahedronLetters,2007,vol.48,#29,p.5055-5060

[10]Patent:EP1212335,2006,B1,.Locationinpatent:Page/Pagecolumn14

[11]ArchivderPharmazie,1997,vol.330,#9-10,p.285-289

[12]Patent:WO2016/172573,2016,A1,.Locationinpatent:Page/Pagecolumn20;21

[13]Tetrahedron,2003,vol.59,#5,p.631-638

[14]Patent:US5436359,1995,A,

545-06-2

92420-89-8

[1]Patent:WO2004/58787,2004,A2,.Locationinpatent:Page29-31

3082-95-9

545-06-2

92420-89-8

[1]ChemicalandPharmaceuticalBulletin,2005,vol.53,#6,p.684-687

[2]JournalofOrganicChemistry,2010,vol.75,#20,p.6747-6755

[3]Synlett,2003,#9SPEC.ISS.,p.1364-1366

[4]CarbohydrateResearch,2004,vol.339,#8,p.1569-1579

[5]Chemicalcommunications(Cambridge,England),2003,#13,p.1518-1519

77668-10-1

545-06-2

92420-89-8

[1]Chemistry-AEuropeanJournal,2011,vol.17,#6,p.1922-1929

3082-96-0

92420-89-8

[1]AngewandteChemie-InternationalEdition,2004,vol.43,#35,p.4653-4656

[2]Patent:WO2016/172573,2016,A1,

Downstream Synthesis Route

100-02-7

92420-89-8

18472-49-6

[1]JournalofOrganicChemistry,1984,vol.49,p.4988-4993

[2]CarbohydrateResearch,2005,vol.340,p.2077-2085

72692-06-9

545-06-2

92420-89-8

[1]CarbohydrateResearch,2003,vol.338,p.2337-2340

[2]MedChemComm,2014,vol.5,p.984-988

[3]JournalofChemicalResearch-PartS,1997,p.370-371

[4]Chemistry-AEuropeanJournal,2020,vol.26,p.1588-1596

[5]CarbohydrateResearch,2012,vol.349,p.108-112

[6]JournalofChemicalCrystallography,2013,vol.43,p.138-143

[7]Steroids,2009,vol.74,p.250-255

[8]JournalofOrganicChemistry,1984,vol.49,p.4988-4993

[9]JournalofOrganicChemistry,2004,vol.69,p.9159-9170

[10]Patent:EP1212335,2006,B1.Locationinpatent:Page/Pagecolumn14

[11]ArchivderPharmazie,1997,vol.330,p.285-289

[12]Patent:WO2016/172573,2016,A1.Locationinpatent:Page/Pagecolumn20;21

[13]Tetrahedron,2003,vol.59,p.631-638

[14]Patent:US5436359,1995,A

[15]OrganicandBiomolecularChemistry,2019,vol.17,p.6970-6974

71939-50-9

92420-89-8

340016-47-9

[1]JournalofMedicinalChemistry,2001,vol.44,p.1467-1470

92420-89-8

619328-24-4

pent-4-enyl2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-α-D-glucopyranoside

[1]Tetrahedron,2003,vol.59,p.631-638

92420-89-8

pent-4-enyl2-azido-2-deoxy-4,6-O-benzylidene-β-D-glucopyranoside

619328-21-1

[1]Tetrahedron,2003,vol.59,p.631-638

Literature

Title: Acetylated methyl glucopyranuronate trichloroacetimidate as a glycosyl donor for efficient synthesis of disaccharides.

Journal: Carbohydrate research 20031031

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SDS