TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Basic information
- Product Name:
- TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
- Synonyms:
-
- TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
- N-BOC-DIETHANOLAMINE
- BOC-DIETHANOLAMINE
- Bis(2-hydroxyethyl)amine, N-BOC protected
- tert-Butyl bis(2-hydroxyethyl)carbamate
- N-Boc-diethanolamine >=98.0% (GC)
- 1-Boc-diethanolamine
- tert-Butyl bis(2-hydroxyethyl)
- CAS:
- 103898-11-9
- MF:
- C9H19NO4
- MW:
- 205.25
- Mol File:
- 103898-11-9.mol
TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Chemical Properties
- Boiling point:
- 324.2±35.0 °C(Predicted)
- Density
- 1.085 g/mL at 20 °C(lit.)
- refractive index
- n20/D 1.461
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 14.29±0.10(Predicted)
- form
- Liquid or Oil
- color
- Colorless
- BRN
- 4386562
- InChI
- InChI=1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
- InChIKey
- KMUNFRBJXIEULW-UHFFFAOYSA-N
- SMILES
- C(OC(C)(C)C)(=O)N(CCO)CCO
- CAS DataBase Reference
- 103898-11-9
MSDS
- Language:English Provider:SigmaAldrich
TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE Usage And Synthesis
Description
tert-butyl bis(2-hydroxyethyl)carbamate is a branched PEG with a tert-butyl protecting group and two hydroxyl end groups. The t-butyl group can be deprotected under acidic conditions. The hydroxyl group can react to further derivatize the compound. The hydrophilic PEG linker increases the water solubility of the compound in aqueous media.
Chemical Properties
Light yellow clear liquid
Uses
Building block for the synthesis of cationic lipids, nucleosides, etc.
reaction suitability
reagent type: cross-linking reagent
Synthesis
24424-99-5
111-42-2
103898-11-9
Under nitrogen protection, 2,2'-Azabisethanol (4.21 g, 40 mmol) was dissolved in acetonitrile (50 mL), and a solution of di-tert-butyl dicarbonate (Boc2O, 9.60 g, 44 mmol) in acetonitrile (50 mL) was slowly added. The reaction mixture was stirred at room temperature for 3.5 h. The solvent was removed by concentration under reduced pressure to afford tert-butyl bis(2-hydroxyethyl)carbamate as a colorless oil (8.20 g, 100% yield).
IC 50
Cleavable Linker; Alkyl/ether
References
[1] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 24, p. 3135 - 3138
[2] Nucleosides and Nucleotides, 1999, vol. 18, # 2, p. 227 - 238
[3] Nucleosides, Nucleotides and Nucleic Acids, 2002, vol. 21, # 2, p. 111 - 123
[4] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 17, p. 4645 - 4665
[5] Patent: WO2014/12360, 2014, A1. Location in patent: Paragraph 00384
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TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE(103898-11-9)Related Product Information
- N-NITROSODIETHYLAMINE
- (2R,4R)-1-tert-Butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
- (2R,4R)-N-Boc-4-hydroxypyrrolidine-2-carboxylic acid
- MORPHOLINE-3,4-DICARBOXYLIC ACID 4-TERT-BUTYL ESTER
- N-Boc-trans-4-tosyloxy-L-proline methyl ester
- TERT-BUTYL N,N-BIS(2-HYDROXYETHYL)CARBAMATE
- N-Boc-trans-4-Hydroxy-L-proline methyl ester
- Boc-Hyp-OH
- N-Boc-cis-4-Hydroxy-L-proline methyl ester
- BOC-HYP(BZL)-OH
- N-Boc-cis-4-Hydroxy-L-proline
- BOC-HYP-OL
- BOC-HYP-OBZL
- BOC-HYP-OH DCHA
- BOC-HYP-OTBU
- BOC-IMINODIACETIC ACID
- BOC-CISHYP(BZL)-OH
- 4(R)-T-BUTYLDIMETHYLSILYLOXY-N-BOC-2(S)PROLINOL