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ChemicalBook >> CAS DataBase List >> t-Boc-Aminoxy-PEG2-alcohol

t-Boc-Aminoxy-PEG2-alcohol

t-Boc-Aminoxy-PEG2-alcohol price.
  • $90 - $2400
  • Product name: t-Boc-Aminoxy-PEG2-alcohol
  • CAS: 1807503-86-1
  • MF: C9H19NO5
  • MW: 221.25
  • EINECS:
  • MDL Number:MFCD28122959
  • Synonyms:t-Boc-Aminoxy-PEG2-alcohol;Boc-Aminooxy-PEG2-alcohol;Boc-Aminoxy-PEG2-OH;t-Boc-Aminooxy-PEG2-alcohol;Boc-Aminooxy-PEG2;Carbamic acid, N-[2-(2-hydroxyethoxy)ethoxy]-, 1,1-dimethylethyl ester;t-Boc-Aminooxy-PEG2-alcoho;t-Boc-Aminooxy-PEG2-alcohol boc
4 prices
Selected condition:
Brand
  • Apolloscientific
  • BroadPharm
  • TRC
Package
  • 10mg
  • 50mg
  • 100mg
  • 5G
  • ManufacturerApolloscientific
  • Product numberBIPG1793
  • Product descriptiont-Boc-Aminoxy-PEG2-alcohol
  • Packaging100mg
  • Price$623
  • Updated2021-12-16
  • Buy
  • ManufacturerBroadPharm
  • Product numberBP-22259
  • Product descriptiont-Boc-Aminooxy-PEG2-alcohol 98%
  • Packaging5G
  • Price$2400
  • Updated2021-12-16
  • Buy
  • ManufacturerTRC
  • Product numberB630318
  • Product descriptionT-Boc-aminoxy-PEG2-alcohol
  • Packaging10mg
  • Price$90
  • Updated2021-12-16
  • Buy
  • ManufacturerTRC
  • Product numberB630318
  • Product descriptionT-Boc-aminoxy-PEG2-alcohol
  • Packaging50mg
  • Price$310
  • Updated2021-12-16
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Apolloscientific BIPG1793 t-Boc-Aminoxy-PEG2-alcohol 100mg $623 2021-12-16 Buy
BroadPharm BP-22259 t-Boc-Aminooxy-PEG2-alcohol 98% 5G $2400 2021-12-16 Buy
TRC B630318 T-Boc-aminoxy-PEG2-alcohol 10mg $90 2021-12-16 Buy
TRC B630318 T-Boc-aminoxy-PEG2-alcohol 50mg $310 2021-12-16 Buy

Properties

Density :1.108±0.06 g/cm3(Predicted)
pka :14.36±0.10(Predicted)
form :Viscous Liquid
color :Colorless to light yellow

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
Precautionary statements:

Description

t-Boc-Aminooxy-PEG2-alcohol is a Boc-protected aminooxy compound. The protected aminooxy can be deprotected under mild acidic conditions and then can react with an aldehyde or ketone group to form a linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.

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