CAS 42969-65-3
:3-Butin-2-olo, (2R)-
- (+)-1-Butyn-3-ol
- (+)-3-Butyn-2-ol
- (2R)-3-Butyn-2-ol
- (2R)-but-3-yn-2-ol
- (R)-(+)-1-Methylpropargyl alcohol
- (R)-1-Butyn-3-ol
- (R)-but-3-yn-2-ol
- 3-Butyn-2-ol, (2R)-
- 3-Butyn-2-ol, (R)-
- (R)-(+)-3-Butyn-2-ol
- (R)-(+)-3-Butyn-2-ol
- Vedi altri sinonimi
(R)-(+)-3-Butyn-2-ol
CAS:Formula:C4H6OPurezza:>98.0%(GC)Colore e forma:Colorless to Light orange to Yellow clear liquidPeso molecolare:70.09(R)-(+)-3-Butyn-2-ol, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C4H6OPurezza:99%Colore e forma:Liquid, Clear colorless to pale yellowPeso molecolare:70.09(2R)-(+)-But-3-yn-2-ol
CAS:(2R)-(+)-But-3-yn-2-ol
Purezza:98%Colore e forma:Colourless To Pale Yellow LiquidPeso molecolare:70.09g/mol(R)-(+)-3-Butyn-2-ol
CAS:(R)-(+)-3-Butyn-2-ol is a chiral alcohol that can be used as a substrate for the synthesis of antibiotics. It has been shown to inhibit phosphatases in vivo and can be used as an inhibitor for phosphatases. (R)-(+)-3-Butyn-2-ol can also be used to synthesize glyoxylate, which is an intermediate for the production of antibiotics. This compound has been shown to have optical activity and stereoselectivity. The synthesis of (R)-(+)-3-butyn-2-ol starts with the alkylation reaction between acetylene and formaldehyde, followed by a cross-coupling reaction with bromoethane and lithium aluminum hydride. The final step is the hydrolysis of furfural using water or lipase, yielding (R)-(+)-3-butyn-2-ol.
Formula:C4H6OPurezza:Min. 98 Area-%Colore e forma:Clear LiquidPeso molecolare:70.09 g/mol




