Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 39885-08-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This bench-stable arylmethanol features a strategically positioned amino group and chlorine substituent, enabling direct incorporation into pharmaceutical intermediates. The para-chloro substitution enhances electrophilic reactivity, while the primary alcohol facilitates derivatization under standard conditions.
(2-Amino-6-chlorophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the aromatic ring and side chain. Its amino and hydroxymethyl groups offer orthogonal reactivity for coupling, derivatization, and heterocycle formation. The compound exhibits good bench stability and facilitates efficient purification, making it suitable for use in multi-step syntheses of bioactive scaffolds and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: