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Chemical Structure| 1234387-33-7 Chemical Structure| 1234387-33-7
Chemical Structure| 1234387-33-7

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Alkyne-PEG2-iodide is a 2-unit PEG derivative with an alkyne group and an iodide group. It is used in click chemistry and bioconjugation reactions.

Synonyms: Alkyne-PEG2-iodide

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Product Details of Alkyne-PEG2-iodide

CAS No. :1234387-33-7
Formula : C7H11IO2
M.W : 254.07
SMILES Code : C#CCOCCOCCI
Synonyms :
Alkyne-PEG2-iodide
MDL No. :MFCD31613942

Safety of Alkyne-PEG2-iodide

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335-H227
Precautionary Statements:P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501

Application In Synthesis of Alkyne-PEG2-iodide

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1234387-33-7 ]

[ 1234387-33-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1119249-30-7 ]
  • [ 1234387-33-7 ]
YieldReaction ConditionsOperation in experiment
92% With potassium iodide; In acetone; for 18h;Reflux; General procedure: A mixture of above obtained tosylate (1.0 eq) andKI (4.0 eq) was refluxed in acetone for 18 hours. Upon completion, excess KI was filtered and washed thrice with acetone. Collected acetone fraction was evaporated under vacuum to get residue, which was then washed with water and extracted with DCM. The combined organic layer was washed with aqueous Na2CO3 and then concentrated under vacuum to get crude product which was purified using silica gel column chromatography using MeORDCM as eluent. Mol. formula: C7H,,021Mol. Weight: 253.95Physical appearance: pale yellow liquidYield: 92% The compound 9c was prepared by general procedure 4.1.3, starting from 9b (1.5 g, 5 mmol), KI (3.3 g, 20 mmol) in acetone. The product was obtained as a pale yellow liquid (1.1 g, 4 mmol, 92%) after purification by silica gel column chromatography using MeOH/DCM as eluent, RrO. 70 in 50% ethyl acetate/hexane. ‘H NMR (400 MHz, CDC13): OH 4.17 (d, J=2.4 Hz, 2H), 3.70-3.63 (m, 7H), 3.57 (t, J=4.4 Hz, 3H), 2.43 (t, J=2.4 Hz, 1H). ‘3C NMR (100 MHz, CDC13): O 79.37, 77.16,74.93, 72.48, 70.17, 69.32, 61.65, 58.41. Mol. formula: C7H,,021Mol. Weight: 253.95Physical appearance: pale yellow liquidYield: 92%
88% With sodium iodide; In acetone; at 20℃; The intermediate (3.0 g, 10 mmol) was dissolved in acetone (40 mL) and treated with sodium iodide (3.0 g, 20 mmol). After stirring at room temperature overnight, the solvent was evaporated and the residue taken up in dichloromethane and water. The organic phase was washed with aqueous sodium thiosulfate solution and water and dried over magnesium sulfate. Concentration furnished 9-iodo-4,7-dioxa-nonyne S3 (2.2 g, 88%) as colourless liquid. 1H NMR (400 MHz, CDCl3): d 4.23 (s, 2H), 3.77 (t, 2H), 3.71 (bs, 4H), 3.28 (t, 2H), 2.45 (bs, 1H); 13C NMR (100 MHz, CDCl3): d 79.51, 74.61, 71.98, 70.00, 69.05, 58.47, 2.67.
 

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