R-4-Chloro-3-hydroxybutyric acid ethyl ester

95%

  • Product Code: 71279
  Alias:    (R) ethyl 4-chloro-3-hydroxybutyrate ; (R) ethyl 4-chloro-3-hydroxybutyrate
  CAS:    90866-33-4
Molecular Weight: 166.6 g./mol Molecular Formula: C₆H₁₁ClO₃
EC Number: MDL Number: MFCD00211242
Melting Point: 93-95 °C Boiling Point: 93-95 °C (5 mmHg)
Density: 1.19 Storage Condition: room temperature
Product Description: This compound is widely used in the synthesis of pharmaceuticals, particularly in the production of chiral intermediates. It serves as a key building block in the development of drugs targeting central nervous system disorders, such as epilepsy and anxiety. Additionally, it is employed in the preparation of beta-blockers, which are essential in managing cardiovascular conditions like hypertension and arrhythmias. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. In research, it is utilized to study enzyme mechanisms and metabolic pathways, particularly those involving hydroxy acids and esters. Its applications also extend to agrochemicals, where it aids in the development of herbicides and fungicides.
Product Specification:
Test Specification
PurityGC 95 100%
PURITYTITRATION WITH AGNO3 95.5 104.5%
REFRACTIVE INDEX N20D 1.451-1.455
SPECIFIC GRAVITY 2020C 1.188-1.192
SPECIFIC ROTATION A20D 12 16
APPEARANCE Colorless to yellow liquid
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿390.00
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-
5.000 10-20 days ฿740.00
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-
25.000 10-20 days ฿2,220.00
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-
100.000 10-20 days ฿8,340.00
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-
R-4-Chloro-3-hydroxybutyric acid ethyl ester
This compound is widely used in the synthesis of pharmaceuticals, particularly in the production of chiral intermediates. It serves as a key building block in the development of drugs targeting central nervous system disorders, such as epilepsy and anxiety. Additionally, it is employed in the preparation of beta-blockers, which are essential in managing cardiovascular conditions like hypertension and arrhythmias. Its chiral nature makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. In research, it is utilized to study enzyme mechanisms and metabolic pathways, particularly those involving hydroxy acids and esters. Its applications also extend to agrochemicals, where it aids in the development of herbicides and fungicides.
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