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Available Variants1 g
CHA.57513-1g
Price
€79.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.57513-1g | €79.80 |
98%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | CH3C6H4SO2NHCH(C6H5)CH(C6H5)NH2 |
|---|---|
| CAS Number | 144222-34-4 |
| Molecular Weight | 366.48 |
| NACRES | NA.22 |
| PubChem Substance ID | 24871941 |
| UNSPSC Code | 12352116 |
| MDL number | MFCD02093428 |
| Assay | 98% |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
(1R,2R)-(−)-N-p-Tosyl-1,2-diphenylethylenediamine, with a CAS number of 144222-34-4, is a chiral diamine compound that has garnered significant attention in the field of organic synthesis. This compound is characterized by its unique stereochemistry, featuring two phenyl groups and a tosyl-protected amine functionality. The (1R,2R) configuration imparts a specific three-dimensional arrangement to the molecule, rendering it a valuable intermediate in the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The tosyl group serves as a protecting group, allowing for selective deprotection and further functionalization of the diamine. As a result, (1R,2R)-(−)-N-p-Tosyl-1,2-diphenylethylenediamine has become a versatile building block in modern organic synthesis, enabling the creation of a wide range of chiral compounds with potential applications in various fields.
