tert-Butyl (4-chloro-3-(trifluoromethyl)phenyl)carbamate

95%

Reagent Code: #130812
fingerprint
CAS Number 352277-93-1

science Other reagents with same CAS 352277-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.69 g/mol
Formula C₁₂H₁₃ClF₃NO₂
badge Registry Numbers
MDL Number MFCD21170395
thermostat Physical Properties
Boiling Point 278.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.320±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the introduction of the tert-butyl carbamate (Boc) protecting group, which is valuable in multi-step organic synthesis for masking amine functionalities. The presence of the trifluoromethyl and chloro substituents enhances lipophilicity and metabolic stability, making it useful in the design of compounds with improved pharmacokinetic properties. Commonly employed in medicinal chemistry for constructing analogs in structure-activity relationship (SAR) studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,500.00
inventory 50mg
10-20 days ฿16,780.00
inventory 100mg
10-20 days ฿26,840.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl (4-chloro-3-(trifluoromethyl)phenyl)carbamate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the introduction of the tert-butyl carbamate (Boc) protecting group, which is valuable in multi-step organic synthesis for masking amine functionalities. The presence of the trifluoromethyl and chloro substituents enhances lipophilicity and metabolic stability, making it useful in the design of compounds with improved pharmacokinetic proper

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the introduction of the tert-butyl carbamate (Boc) protecting group, which is valuable in multi-step organic synthesis for masking amine functionalities. The presence of the trifluoromethyl and chloro substituents enhances lipophilicity and metabolic stability, making it useful in the design of compounds with improved pharmacokinetic properties. Commonly employed in medicinal chemistry for constructing analogs in structure-activity relationship (SAR) studies.

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...