(R)-()-2-(tert-butoxycarbonylamino)-3-phenylprop

98%

Reagent Code: #53843
fingerprint
CAS Number 77119-85-8

science Other reagents with same CAS 77119-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.31 g/mol
Formula C₁₄H₁₉NO₃
badge Registry Numbers
MDL Number MFCD00274187
thermostat Physical Properties
Melting Point 86-89℃
Boiling Point 367℃ at 760 mmHg
inventory_2 Storage & Handling
Storage -20℃, inert gas, sealed

description Product Description

This chemical is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the preparation of chiral compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure allows for the introduction of phenylalanine derivatives, which are crucial in creating biologically active molecules. Additionally, it is employed in asymmetric synthesis to produce enantiomerically pure substances, enhancing the efficacy and specificity of therapeutic agents. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during complex chemical reactions, making it valuable in organic and medicinal chemistry research.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White to Light Yellow Solid
Purity (%) 97.5-100%
Specific Rotation [α]20/D (c=0.5 in MeOH) (°) 41-49
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿16,515.00
inventory 250mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿3,897.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-()-2-(tert-butoxycarbonylamino)-3-phenylprop
No image available
This chemical is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the preparation of chiral compounds, particularly in the development of drugs targeting neurological and cardiovascular disorders. Its structure allows for the introduction of phenylalanine derivatives, which are crucial in creating biologically active molecules. Additionally, it is employed in asymmetric synthesis to produce enantiomerically pure substances, enhancing the efficacy and specificity of therapeutic agents. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during complex chemical reactions, making it valuable in organic and medicinal chemistry research.
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...