| N-(3-Indolylacetyl)-L-isoleucine Basic information |
| Product Name: | N-(3-Indolylacetyl)-L-isoleucine |
| Synonyms: | IAA-L-ILE;INDOLE-3-ACETYL-L-ISOLEUCINE;N-(3-INDOLYLACETYL)-L-ISOLEUCINE;N-(3-Indolylacetyl)-L-isoleucine, Indole-3-acetyl-L-isoleucine, 99%;INDOLE-3-ACETYL-L-ISOLEUCINE (IAIleu);(2S,3R)-2-[[2-(1H-indol-3-yl)-1-oxoethyl]amino]-3-methylpentanoic acid;L-Isoleucine, N-[2-(1H-indol-3-yl)acetyl]-;N-(3-Indolylacetyl)-L-isoleucine USP/EP/BP |
| CAS: | 57105-45-0 |
| MF: | C16H20N2O3 |
| MW: | 288.34 |
| EINECS: | |
| Product Categories: | Indoles and derivatives;Leucine Derivatives;Peptide Synthesis;Unnatural Amino Acid Derivatives |
| Mol File: | 57105-45-0.mol |
| N-(3-Indolylacetyl)-L-isoleucine Chemical Properties |
| Melting point | 182-183 °C(lit.) |
| optical activity | [α]20/D +6°, c = 3 in methanol |
| Safety Information |
| WGK Germany | 3 |
| HS Code | 29339980 |
| MSDS Information |
| Provider | Language |
|---|---|
| SigmaAldrich | English |
| N-(3-Indolylacetyl)-L-isoleucine Usage And Synthesis |
| Uses | Indole-3-acetyl-L-isoleucine is an indole-3-acetyl-amino acid conjugate involved in regulatory mechanisms for the control of auxin activity during physiological and pathophysiological responses. |
| N-(3-Indolylacetyl)-L-isoleucine Preparation Products And Raw materials |
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