Ordering
Available Variants250 mg
CHA.90464-250mg
Price
€114.40
Available – Dispatch in 14 days
1 g
CHA.90464-1g
Price
€440.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
250 mg | CHA.90464-250mg | €114.40 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.90464-1g | €440.80 |
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
| Empirical Formula (Hill Notation) | C13H24N2O3 |
|---|---|
| CAS Number | 119838-38-9 |
| Molecular Weight | 256.34 |
| UNSPSC Code | 12352200 |
| NACRES | NA.22 |
| PubChem Substance ID | 24860488 |
| MDL number | MFCD00075101 |
| Beilstein/REAXYS Number | 4907144 |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
(S)-(−)-1-Boc-2-tert-butyl-3-methyl-4-imidazolidinone, with the CAS registry number 119838-38-9, is a chiral auxiliary commonly utilized in organic synthesis. This compound is a derivative of imidazolidinone, which is a five-membered ring structure containing two nitrogen atoms. The presence of the tert-butyl group and the methyl group attached to the imidazolidinone ring provides a unique steric environment, making it useful for asymmetric synthesis. The Boc (tert-butoxycarbonyl) group serves as a protecting group, allowing for the selective deprotection and further functionalization of the molecule. This compound has been employed in various reactions, including asymmetric alkylations and aldol reactions, to produce enantiomerically enriched products. Its utility in organic synthesis stems from its ability to induce high levels of stereoselectivity in a wide range of transformations.
