N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL
N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Basic information
- Product Name:
- N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL
- Synonyms:
-
- 1,1-DINEOPENTYLOXYTRIMETHYLAMINE
- 1,1-bis(2,2-dimethylpropoxy)-N,N,N-trimethylamine
- Methanamine, 1,1-bis(2,2-dimethylpropoxy)-N,N-dimethyl-
- 1,1-dineopentyloxy-n,n-dimethylmethylamine
- N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL
- N,N-Dimethyl[bis(neopentyloxy)]methanamine
- Dimethylformamide dineopentyl acetal.
- N,N-Dimethylformamide Dineopentyl Acetal [for Esterification]
- CAS:
- 4909-78-8
- MF:
- C13H29NO2
- MW:
- 231.37
- EINECS:
- 225-536-4
- Product Categories:
-
- Analytical Chemistry
- Esterification & Alkylation (GC Derivatizing Reagents)
- GC Derivatizing Reagents
- N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents)
- Mol File:
- 4909-78-8.mol
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N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Chemical Properties
- Melting point:
- 253.5℃
- Boiling point:
- 85-87 °C/10 mmHg (lit.)
- Density
- 0.829 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.412(lit.)
- Flash point:
- 125 °F
- storage temp.
- Store at 0-5°C
- pka
- 5.24±0.50(Predicted)
- form
- clear liquid
- color
- Colorless to Almost colorless
- Water Solubility
- Hydrolyzes with water.
- Sensitive
- Moisture Sensitive
- BRN
- 741992
- CAS DataBase Reference
- 4909-78-8(CAS DataBase Reference)
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MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Usage And Synthesis
Chemical Properties
Colorless to slight yellow liquid
Uses
N,N-Dimethylformamide dineopentyl acetal helps in the lactonization of ω-hydroxyacids, giving lactones of up to 16-membered rings. It can be used to convert primary alcohols to alkylating agents for use in the alkylation of thiols. It is used in the esterification of Nα-9-fluorenylmethyloxycarbonylamino acids. It was used in the synthesis of 1,3-dialkyl, benzyl and cyclohexyl barbiturate derivatives. It was used as reagent during the synthesis of L-serine and L-cystine stereospecifically labeled with deuterium at the β-position.
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