N-Acetyl-D-alaninol
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| Category | Others |
| Catalog number | BBF-05176 |
| CAS | 145842-51-9 |
| Molecular Weight | 117.15 |
| Molecular Formula | C5H11NO2 |
| Purity | >95% by HPLC |
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Specification
| Related CAS | 35593-62-5 (L-configuration) |
| Synonyms | Acetamide, N-[(1R)-2-hydroxy-1-methylethyl]-; (R)-N-(1-Hydroxypropan-2-yl)acetamide; (+)-N-[(R)-2-Hydroxy-1-methylethyl]acetamide |
| Storage | Store at -20°C |
| IUPAC Name | N-[(2R)-1-hydroxypropan-2-yl]acetamide |
| Canonical SMILES | CC(CO)NC(=O)C |
| InChI | InChI=1S/C5H11NO2/c1-4(3-7)6-5(2)8/h4,7H,3H2,1-2H3,(H,6,8)/t4-/m1/s1 |
| InChI Key | LFVBTAFBWUVUHV-SCSAIBSYSA-N |
Properties
| Boiling Point | 304.7±25.0°C at 760 mmHg |
| Density | 1.0±0.1 g/cm3 |
Reference Reading
1. Synthesis of the C(21)-C(26) fragment of superstolide A: concerning the stereochemistry of (E)-crotylboration reactions of alaninal derivatives
Neal A Yakelis, William R Roush J Org Chem. 2003 May 16;68(10):3838-43. doi: 10.1021/jo0341012.
A stereoselective synthesis of the C(21)-C(26) fragment of superstolide A has been completed. The absolute and relative stereochemistry of intermediate 14 has been conclusively proven by NMR and X-ray diffraction methods. In the course of this work, it was found that the stereochemistry of 3 had been misassigned in our previously reported synthesis of the C(18)-C(26) segment. This error stems from the unexpected diastereoselectivity in the double asymmetric reaction of N-acetyl-d-alaninal 1 and the tartrate ester modified (E)-crotylboronate (R,R)-2.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
