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Key Documents

06023

Sigma-Aldrich

Allylmalonic acid

≥98.0% (T)

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About This Item

Linear Formula:
CH2=CHCH2CH(COOH)2
CAS Number:
Molecular Weight:
144.13
Beilstein/REAXYS Number:
1766382
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥98.0% (T)

form

powder

mp

102-105 °C

functional group

allyl
carboxylic acid

SMILES string

OC(=O)C(CC=C)C(O)=O

InChI

1S/C6H8O4/c1-2-3-4(5(7)8)6(9)10/h2,4H,1,3H2,(H,7,8)(H,9,10)

InChI key

ZDZVKPXKLLLOOA-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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W Zou et al.
Glycoconjugate journal, 16(9), 507-515 (2000-05-18)
A biantennary GM3-saccharide (sialyllactoside) derivative (4) was constructed using allylmalonic acid as a bivalent linker, both carboxylic acids of which were condensed with 3-aminopropyl lactoside (2) prior to enzymatic sialylation with a fusion enzyme. While ozonolysis of its allyl group

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