N-Boc-2-aminoacetaldehyde
ALDRICH/472654 - 95%
Synonym: tert-Butyl N-
CAS Number: 89711-08-0
Empirical Formula (Hill Notation): C7H13NO3
Molecular Weight: 159.18
MDL Number: MFCD01321273
Linear Formula: HCOCH2NHCO2C(CH3)3
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 472654-25G
| assay | 95% |
| InChI | 1S/C7H13NO3/c1-7(2,3)11-6 |
| InChI key | ACNRTYKOPZDRCO-UHFFFAOYSA |
| Quality Level | 100  |
| refractive index | n |
| SMILES string | CC(C)(C)OC(=O)NCC=O |
| storage temp. | −20°C |
| Application: | N-Boc-2-aminoacetaldehyde may be employed in the following: • As a starting reagent in the total synthesis of (+)-negamycin. • Synthesis of (E)-ethyl 4-((tert-butoxycarbonyl)amino)but • Synthesis of 2,2′-bipyridine. |
| Application: | A building block in the synthesis of a protected pyrroloproline. |
| Application: | α-Methylenation of this amino aldehyde proceeds in a quick and efficient manner using a recently reported protocol involving formaldehyde and catalysis by either pyrrolidine proprionic acid or the dipeptide L-Pro-β-Ala. Also used in a three-component synthesis of pyrrolidines involving 1,3-dipolar cycloaddition. |
| General description: | N-Boc-2-aminoacetaldehyde is an organic building block. It reacts with Horner-Wadsworth-Emmons (HWE) reagent to afford γ-aminobutyric acid (GABA)-derived α-keto amide/ester units. |
| Packaging: | 1, 5, 25 g in glass bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | 235.4 °F - closed cup |
| Flash Point(C) | 113 °C - closed cup |
| Purity | 95% |
| Refractive Index | n |
| Storage Temp. | −20°C |
| UNSPSC | 12352100 |