methyl N-[(3S,4S)-4-methylpiperidin-3-yl]carbamate

≥95%

Reagent Code: #220359
fingerprint
CAS Number 694495-64-2

science Other reagents with same CAS 694495-64-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.23 g/mol
Formula C₈H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD31618478
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of centrally acting drugs. Its structure supports binding to neurological targets, making it valuable in creating compounds for cognitive and psychiatric disorders. Commonly employed in the preparation of selective receptor modulators due to its favorable stereochemistry and ability to enhance blood-brain barrier penetration. Also utilized in medicinal chemistry research for optimizing drug candidates with improved metabolic stability and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿44,090.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
methyl N-[(3S,4S)-4-methylpiperidin-3-yl]carbamate
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of centrally acting drugs. Its structure supports binding to neurological targets, making it valuable in creating compounds for cognitive and psychiatric disorders. Commonly employed in the preparation of selective receptor modulators due to its favorable stereochemistry and ability to enhance blood-brain barrier penetration. Also utilized in medicinal chemistry research for optimizing drug candidates wi

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of centrally acting drugs. Its structure supports binding to neurological targets, making it valuable in creating compounds for cognitive and psychiatric disorders. Commonly employed in the preparation of selective receptor modulators due to its favorable stereochemistry and ability to enhance blood-brain barrier penetration. Also utilized in medicinal chemistry research for optimizing drug candidates with improved metabolic stability and bioavailability.

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...