[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid
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![[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/5d0bb07800bf4c25b5b7eff53749ba75.png "[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid")
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid
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CAS No:
49669-74-1
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Formula:
C6H12N2O3
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Chemical Name:
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid
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Synonyms:
(2S,3E)-2-Amino-4-(2-aminoethoxy)-3-butenoic acid;Ro-4468;TMP-941;Antibiotic ro 20-4468/001;Nsc234613;Ro 20-4468/001;[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid;USGUVNUTPWXWBA-JRIXXDKMSA-N
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CAS No:
Description
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid is produced by Streptomyces spp. and was isolated and purified by Abbott. It is marketed by Valent Biosciences for control of fruit ripening as it inhibits the production of endogenous ethylene.
Characteristics
98.57000
0.28790
1.232±0.06 g/cm3(Predicted)
363.7±42.0 °C(Predicted)
173.7ºC
1.531
1.50±0.10(Predicted)
[S-(E)]-2-amino-4-(2-aminoethoxy)-3-butenoic acid Use and Manufacturing
Aviglycine (ABG-3168 free base) is an inhibitor of ethylene biosynthesis with antibacterial activity. Aviglycine (ABG-3168 (free base)) application delays natural flowering in pineapple[1].
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