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Chemical Structure| 920264-35-3 Chemical Structure| 920264-35-3

Structure of t-Boc-N-amido-PEG2-C6-Cl
CAS No.: 920264-35-3

Chemical Structure| 920264-35-3

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Product Details of [ 920264-35-3 ]

CAS No. :920264-35-3
Formula : C15H30ClNO4
M.W : 323.86
SMILES Code : O=C(OC(C)(C)C)NCCOCCOCCCCCCCl
MDL No. :MFCD31568195

Safety of [ 920264-35-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 920264-35-3 ]

* 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 [ 920264-35-3 ]

[ 920264-35-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 920264-35-3 ]
  • [ 1035373-85-3 ]
YieldReaction ConditionsOperation in experiment
98% With hydrogenchloride; In 1,4-dioxane; at 20℃; for 2h; 700 mg (2.16 mmol, 1.0 eq) product of step 14.3 was dissolved in 2.5 mL 4 M HC1 in dioxane (9.73 mmol, 4.55 eq) and was stirred at room temperature for 2 hours. The solvent was removed in vacuum and the product was obtained as white solid, which was used without further purification.
With hydrogenchloride; In 1,4-dioxane; at 20℃; for 1h; Commercially available chloro- alcohol was converted into tosylate. Condition (a) 6-Chloro-l-hexanol (1.0 eq.), p- Toluenesulfonyl chloride (1.1 eq), 4-dimethylaminopyridine (0.1 eq) in pyridine for 1.5 hours at 0C. The reaction mixture was extracted with diethyl ether against diluted HC1. The organic phase was collected and evaporated under reduced pressure, yielding crude colorless crystal 6. The product was carried on to the next step without further purification. Commercially available amino-alcohol was protected with t-butyl carbonate group. Condition (b) 2-(2- (0303) Aminoethoxy)ethanol (1.0 eq.), Di-tert-butyl dicarbonate (1.0 eq.) in methanol stirred for 3 h at room temperature. The reaction mixture was extracted with PBS Buffer against dichloromethane. The organic fraction was dried in vacuo. Compounds were further purified by flash chromatography (1 :1 ethyl acetate/hexane) to yield 7, a colorless oil. 6 and 7 were combined to become protected PEG linker. Condition (c) 6 (1 eq), 7 (1.1 eq), and Potassium tert-butoxide (1 M in THF, 1.5 eq) in DMF stirred overnight at room temperature. The reaction was quenched with water and extracted with diethyl ether. The product was further purified by flash chromatography (1 :2 ethyl acetate: hexane). Colorless oil 8 was obtained. Deprotection of 8 yielded the PEG amine hydrochloride. Condition (d) 8 (1 eq), HC1 (4 M in Dioxane, 6 eq) stirred for 1 h at room temperature. Concentrated and then dried under high-vac to yield 9 a white solid.
With hydrogenchloride; In 1,4-dioxane; at 20℃; for 1h; Add 1 equivalent of compound 8, 6 equivalents of HCl (4M in Dioxane) at room temperature, and mix and stir for 1 h. After the reaction is complete, filter with suction and dry in vacuo to obtain a white solid, namely compound 9
 

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