(S)-Methyl 2,3-diaminopropanoate dihydrochloride

97%

Reagent Code: #38004
fingerprint
CAS Number 147857-43-0

science Other reagents with same CAS 147857-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.0563 g/mol
Formula C₄H₁₂Cl₂N₂O₂
badge Registry Numbers
MDL Number MFCD09998031
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(S)-Methyl 2,3-diaminopropanoate dihydrochloride is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. Its stereochemistry makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It serves as a precursor in the production of various biologically active molecules, including peptides and enzyme inhibitors, where the (S)-configuration is critical for activity. Additionally, it is employed in research settings for studying stereochemical reactions and developing new synthetic methodologies. Its application extends to the field of medicinal chemistry, where it aids in the design of drugs targeting specific biological pathways with high selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,593.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-Methyl 2,3-diaminopropanoate dihydrochloride
No image available

(S)-Methyl 2,3-diaminopropanoate dihydrochloride is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. Its stereochemistry makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It serves as a precursor in the production of various biologically active molecules, including peptides and enzyme inhibitors, where the (S)-configuration is critical for activity. Additionally, it is empl

(S)-Methyl 2,3-diaminopropanoate dihydrochloride is primarily utilized in organic synthesis as a chiral building block for the preparation of complex molecules. Its stereochemistry makes it valuable in the development of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It serves as a precursor in the production of various biologically active molecules, including peptides and enzyme inhibitors, where the (S)-configuration is critical for activity. Additionally, it is employed in research settings for studying stereochemical reactions and developing new synthetic methodologies. Its application extends to the field of medicinal chemistry, where it aids in the design of drugs targeting specific biological pathways with high selectivity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...