ChemicalBook > CAS DataBase List > N-(3-Indolylacetyl)-L-isoleucine

N-(3-Indolylacetyl)-L-isoleucine

Product Name
N-(3-Indolylacetyl)-L-isoleucine
CAS No.
57105-45-0
Chemical Name
N-(3-Indolylacetyl)-L-isoleucine
Synonyms
IAA-L-ILE;INDOLE-3-ACETYL-L-ISOLEUCINE;N-(3-INDOLYLACETYL)-L-ISOLEUCINE;INDOLE-3-ACETYL-L-ISOLEUCINE (IAIleu);N-(3-Indolylacetyl)-L-isoleucine USP/EP/BP;L-Isoleucine, N-[2-(1H-indol-3-yl)acetyl]-;N-(3-Indolylacetyl)-L-isoleucine, Indole-3-acetyl-L-isoleucine, 99%;(2S,3R)-2-[[2-(1H-indol-3-yl)-1-oxoethyl]amino]-3-methylpentanoic acid
CBNumber
CB7777284
Molecular Formula
C16H20N2O3
Formula Weight
288.34
MOL File
57105-45-0.mol
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N-(3-Indolylacetyl)-L-isoleucine Property

Melting point:
182-183 °C(lit.)
optical activity
[α]20/D +6°, c = 3 in methanol
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Safety

WGK Germany 
3
HS Code 
29339980
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
I577385
Product name
Indole-3-acetyl-L-isoleucine
Packaging
100mg
Price
$140
Updated
2021/12/16
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N-(3-Indolylacetyl)-L-isoleucine Chemical Properties,Usage,Production

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

Raw materials

Preparation Products

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N-(3-Indolylacetyl)-L-isoleucine Suppliers

BIOSYNTH AG
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Biosynth AG
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57105-45-0, N-(3-Indolylacetyl)-L-isoleucineRelated Search:


  • 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
  • 57105-45-0
  • Unnatural Amino Acid Derivatives
  • Specialty Synthesis
  • Peptide Synthesis
  • Leucine Derivatives
  • Indoles and derivatives
  • Leucine Derivatives
  • Peptide Synthesis
  • Unnatural Amino Acid Derivatives