| Bioactivity | N-benzoyl-L-aspartic acid, a major metabolite of benzyl glucosinolate, can be used for modification of peptides or proteins[1]. | ||||||||||||
| Invitro | N-benzoyl-L-aspartic acid resists racemisation by aqueous acetic anhydride and evidence is adduced to show that they form internal anhydrides rather than oxazolones under these conditions[2]. | ||||||||||||
| Name | N-benzoyl-L-aspartic acid | ||||||||||||
| CAS | 4631-12-3 | ||||||||||||
| Formula | C11H11NO5 | ||||||||||||
| Molar Mass | 237.21 | ||||||||||||
| Appearance | Solid | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
|
||||||||||||
| Reference | [1]. Friedrichs J, et, al. Novel glucosinolate metabolism in larvae of the leaf beetle Phaedon cochleariae. Insect Biochem Mol Biol. 2020 Sep;124:103431. [2]. BARKER CC, et, al. The Dehydration and Racemisation of N-Acyl-L-aspartic Acids by Acetic Anhydride. Journal of the Chemical Society. 1953. |
N-benzoyl-L-aspartic acid
CAS: 4631-12-3 F: C11H11NO5 W: 237.21
N-benzoyl-L-aspartic acid, a major metabolite of benzyl glucosinolate, can be used for modification of peptides or prote
Sales Email：peptidedb@qq.com
This product is for research use only, not for human use. We do not sell to patients.