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Available Variants25 g
CHA.66113-25g
Price
€84.00
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.66113-25g | €84.00 |
≥99%
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 | [CH(OH)CONHCH2CH=CH2]2 |
|---|---|
| CAS Number | 58477-85-3 |
| Molecular Weight | 228.25 |
| UNSPSC Code | 12352002 |
| NACRES | NA.22 |
| PubChem Substance ID | 24849641 |
| EC Number | 261-277-3 |
| Beilstein/REAXYS Number | 1712934 |
| MDL number | MFCD00008640 |
| Assay | ≥99% |
Safety Information Handling visibility
| 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
(+)-N,N′-Diallyltartramide, with the CAS registry number 58477-85-3, is a synthetic organic compound that has garnered significant attention in various fields of research. This chiral diamide is derived from tartaric acid and has been utilized as a versatile building block in the synthesis of complex molecules. Its unique structural features make it an attractive intermediate for the preparation of biologically active compounds and chiral ligands. The compounds properties and reactivity have been extensively studied, and it has been employed in numerous asymmetric synthesis protocols. Furthermore, (+)-N,N′-Diallyltartramide has been used as a chiral auxiliary in various reactions, including cycloadditions and hydrogenations, allowing for the efficient introduction of chirality into target molecules. Its applications continue to expand, driven by the growing demand for enantiopure compounds in pharmaceutical and materials science.
