Ordering
Available Variants1 g
CHA.11406-1g
Price
€75.68
Available – Dispatch in 14 days
5 g
CHA.11406-5g
Price
€27.48
Available – Dispatch in 14 days
25 g
CHA.11406-25g
Price
€38.32
Available – Dispatch in 14 days
100 g
CHA.11406-100g
Price
€145.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.11406-1g | €75.68 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.11406-5g | €27.48 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.11406-25g | €38.32 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.11406-100g | €145.60 |
99%, for peptide synthesis
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 | (CH3)3COCOON=C(C6H5)CN |
|---|---|
| CAS Number | 58632-95-4 |
| Molecular Weight | 246.26 |
| NACRES | NA.22 |
| PubChem Substance ID | 24851592 |
| UNSPSC Code | 12352108 |
| EC Number | 261-370-9 |
| MDL number | MFCD00001863 |
| Beilstein/REAXYS Number | 2217296 |
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
2-(Boc-oxyimino)-2-phenylacetonitrile, also known by its CAS number 766-46-1, is a chemical compound that has garnered significant attention in the realm of organic synthesis. This compound is a protected oxime, where the Boc group serves as a tert-butyl carbamate protecting group, and it is widely utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. The presence of the nitrile group and the phenyl ring in its structure makes it a versatile building block for the construction of complex molecules. Additionally, the Boc protecting group can be easily removed under acidic conditions, making it a convenient choice for synthetic chemists. As a result, 2-(Boc-oxyimino)-2-phenylacetonitrile has become a valuable tool in the field of organic chemistry, enabling the efficient synthesis of a wide range of biologically active compounds.
