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Merck
CN

794449

Sigma-Aldrich

6-O-Acryloyl-1,2:3,4-bis-O-(1-methylethylidene)-α-D-galactopyranose

contains MEHQ as inhibitor

Synonym(s):

1,2:3,4-Di-O-isopropylidene-6-O-acryloyl-α-D-galactopyranose, AGP, protected pyranose acrylate

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About This Item

Empirical Formula (Hill Notation):
C15H22O7
CAS Number:
2715-35-7
Molecular Weight:
314.33
UNSPSC Code:
12162002
PubChem Substance ID:
329768449

Key Documents

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form

powder

contains

MEHQ as inhibitor

mp

47-52 °C

storage temp.

2-8°C

SMILES string

CC1(O[C@@H]([C@H]([C@@H](COC(C=C)=O)O2)O1)[C@@H](O3)[C@H]2OC3(C)C)C

InChI

1S/C15H22O7/c1-6-9(16)17-7-8-10-11(20-14(2,3)19-10)12-13(18-8)22-15(4,5)21-12/h6,8,10-13H,1,7H2,2-5H3/t8-,10+,11+,12-,13-/m1/s1

InChI key

PVHFRWORCBIGDM-UUWLPUTASA-N

Application

This monomer can be used to make macromolecules containing carbohydrate moieties. Controlled Radical Polymerization; such as NMP, RAFT, or ATRP, is commonly employed to synthesize well-defined glycopolymers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBV1689V

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S R Simon Ting et al.
Biomacromolecules, 10(2), 342-352 (2009-01-23)
Hollow poly(6-O-acryloyl-alpha-D-galactopyranose) (PAGP) nanospheres were prepared in a facile manner using the RAFT (reversible addition fragmentation chain transfer) process. Initially, an amphiphilic block copolymer, poly(lactide)-block-poly(6-O-acryloyl-alpha-D-galactopyranose) (PLA-b-PAGP), was synthesized using a poly(lactide) (PLA) macroRAFT agent. It was attained in high yields

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