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ChemicalBook--->CAS DataBase List--->214467-60-4

214467-60-4

214467-60-4 Structure

214467-60-4 Structure
IdentificationBack Directory
[Name]

2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE
[CAS]

214467-60-4
[Synonyms]

GlcNPhth[36Bn,4Ac]-beta-MP
-D-glucopyranosyl Azide
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-&beta
2-Acetamido-2-deoxy-beta-D-glucopyranosylaminobiotin
2-Acetamido-N-biotinyl-2-deoxy-beta-D-glucopyranosylamine
2,4,7,8,9-Penta-O-acetyl-N-acetylneuraminic Acid Methyl Ester
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-b-D-glucopyranosylazide
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl azide
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosyl azide
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranosylAzide>
2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE
N-[2-AZIDO-4,5-BIS(BENZYLOXY)-6-[(BENZYLOXY)METHYL]OXAN-3-YL]ACETAMIDE
2-ACETAMIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE USP/EP/BP
2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl azide >=98.0% (HPLC)
N-[(2R,3R,4R,5S,6R)-2-azido-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-3-yl]acetamide
Methyl 5-Acetamido-2,4,7,8,9-penta-O-acetyl-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosylonate
[Molecular Formula]

C29H32N4O5
[MDL Number]

MFCD06797049
[MOL File]

214467-60-4.mol
[Molecular Weight]

516.59
Chemical PropertiesBack Directory
[Melting point ]

105 °C
[refractive index ]

6 ° (C=1, CHCl3)
[storage temp. ]

Freezer
[form ]

powder to crystal
[color ]

White to Almost white
[optical activity]

[α]/D 5.0±0.5°, c = 1 in chloroform
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29329990
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder or crystal
[Uses]

2-Acetamido-3,4,6-tri-O-benzyl-2-deoxy-beta-D-glucopyranosyl Azide (CAS# 214467-60-4) is a glycosyl azide used in the preparation of nonglycosylated androgenic gland hormone (AGH) and glycosylated AGH with N-linked glycan using expressed protein ligation.
[reaction suitability]

reaction type: click chemistry
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