57105-39-2

57105-39-2 structure

Name: N-(3-Indolylacetyl)-L-alanine
Chemical Name: (2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]propanoic acid
CAS Number: 57105-39-2
Molecular Formula: C₁₃H₁₄N₂O₃
Molecular Weight: 246.26200
Catalog: Biochemical Amino acids and their derivatives Alanine derivatives
Create Date: 2018-12-08 17:06:14
Modify Date: 2024-01-14 12:06:52
N-(3-Indolylacetyl)-L-alanine (Indoleacetylalanine) is an indoleacetylamino acid. N-(3-Indolylacetyl)-L-alanine appears to increase callus growth and reduces the ability of growths to differentiate into shoots of Phalaenopsis orchids[1].

Name	(2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]propanoic acid
Synonyms	L-Alanine,N-(1H-indol-3-ylacetyl)-(9CI) Alanine,N-indol-3-ylacetyl-(6CI) Indole-3-acetylalanine N-(3-Indolylacetyl)-L-alanine (S)-2-(2-(1H-indol-3-yl)acetamido)propanoic acid IAA-L-Ala Indole-3-acetyl-L-alanine Alanine,N-(3-indolylacetyl) MFCD00050395 IAA-L-Ala-OH IAA-Ala N-(indol-3-ylacetyl)-L-alanine L-alanine,N-(1H-indol-3-ylacetyl) N-(3-Indolylacetyl)-L-alanine

Description	N-(3-Indolylacetyl)-L-alanine (Indoleacetylalanine) is an indoleacetylamino acid. N-(3-Indolylacetyl)-L-alanine appears to increase callus growth and reduces the ability of growths to differentiate into shoots of Phalaenopsis orchids[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
References	[1]. Griesbach R J. The use of indoleacetylamino acids in the in vitro propagation of Phalaenopsis orchids. Scientia Horticulturae, 1983, 19(3-4): 363-366.

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RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2933990090

56-41-7

1080025-88-2

~63%

57105-39-2

Precursor 2
56-41-7 1080025-88-2
DownStream 0

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%