Ordering
Available Variants1 g
CHA.74482-1g
Price
€71.44
Available – Dispatch in 14 days
5 g
CHA.74482-5g
Price
€180.80
Available – Dispatch in 14 days
10 g
CHA.74482-10g
Price
€263.20
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.74482-1g | €71.44 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.74482-5g | €180.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
10 g | CHA.74482-10g | €263.20 |
≥95%
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) | C18H20BNO |
|---|---|
| CAS Number | 112022-81-8 |
| Molecular Weight | 277.17 |
| NACRES | NA.22 |
| PubChem Substance ID | 24883643 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD00078439 |
Safety Information Handling visibility
| pictograms |
GHS05
GHS07
  GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H302,H318 |
| Hazard Classifications | Acute Tox. 4 Oral - Eye Dam. 1 |
| Storage Class | 11 - Combustible Solids |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
| pcodes | P264 - P270 - P280 - P301 + P312 - P305 + P351 + P338 - P501 |
Technical Overview & Applications Use-case context
(S)-(−)-2-Methyl-CBS-oxazaborolidine, with the CAS number 67-07-2, is a chiral organoborane compound that has been widely utilized as a catalyst in asymmetric synthesis. This oxazaborolidine derivative is known for its high efficiency and selectivity in promoting various organic transformations, including reductions and alkylations. The (S)-enantiomer of 2-Methyl-CBS-oxazaborolidine is particularly effective in facilitating the enantioselective reduction of prochiral ketones to form chiral alcohols. Its utility in organic synthesis stems from its ability to form a borane complex that can selectively bind to one face of a prochiral substrate, thereby inducing high stereoselectivity in the resulting product. As a result, (S)-(−)-2-Methyl-CBS-oxazaborolidine has become a valuable tool in the field of asymmetric catalysis, enabling the efficient preparation of enantiopure compounds that are essential in pharmaceutical and agrochemical applications.
