Description of CAS: 155976-13-9|Boc-L-cyclopropylglycine
| 155976-13-9 | |
| C10H17NO4 | |
| 215.25 | |
| 364.7±25.0 degree (Predicted) | |
|
1.206±0.06 g/cm3(Predicted) |
|
| 79 degree | |
| 97% | |
| 250mg 1g 5g 10g 25g 50g 100g 1kg 5kg |
(S)-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID;
(2S)-cyclopropyl ({[(1,1-dimethylethyl)oxy]carbonyl}amino)ethanoic acid;
(2S)-[(tert-Butoxycarbonyl)amino](cyclopropyl)acetic acid;
(2S)-[(tert-butoxycarbonyl)amino](cyclopropyl)ethanoic acid;
(S)-TERT-BUTOXYCARBONYLAMINO-CYCLOPROPYL-ACETIC ACID;
(S)-2-tert-butoxycarbonylamino-2-cyclopropylacetic acid;
Boc-L-Cyclopropylglycine;
N-tert-Butoxycarbonyl-L-cyclopropylglycine;
(R)-2-(N-tert-butoxycarbonylamino)-2-cyclopropylacetic acid;
L-Cyclopropylglycine,N-BOC protected;
(S)-Amino(cyclopropyl)acetic acid,N-BOC protected;
Boc-(S)-2-cyclopropylglycine;
BOC-(2S)-GLY(2-CYCLOPROPYL);
Boc-l-cyclopropyl glycine has been widely used in drug research and organic synthesis. As a type of amino acid, it can be used to synthesize peptides and proteins. Its protective group Boc can protect the active hydrogen atoms on the amino group during chemical reactions to avoid unnecessary reactions. Boc-l-cyclopropyl glycine can also be used as a building block of drug molecules for the synthesis of antibiotics, anti-tumor drugs, and other bioactive compounds.
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