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57105-39-2

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57105-39-2 Usage

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Indole-3-acetic-L-alanine is a derivative of the phytohormone indole-3-acetic acid (I577340) used in studies for the isolation and characterization of Arabdopsis thaliana mutants.

Check Digit Verification of cas no

The CAS Registry Mumber 57105-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,0 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57105-39:
(7*5)+(6*7)+(5*1)+(4*0)+(3*5)+(2*3)+(1*9)=112
112 % 10 = 2
So 57105-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O3/c1-8(13(17)18)15-12(16)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7-8,14H,6H2,1H3,(H,15,16)(H,17,18)/t8-/m0/s1

57105-39-2 Well-known Company Product Price

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  • Aldrich

  • (345911)  N-(3-Indolylacetyl)-L-alanine  98%

  • 57105-39-2

  • 345911-250MG

  • 500.76CNY

  • Detail

57105-39-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[2-(1H-indol-3-yl)acetyl]amino]propanoic acid

1.2 Other means of identification

Product number -
Other names N-(3-Indolylacetyl)-L-alanine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57105-39-2 SDS

57105-39-2Downstream Products

57105-39-2Relevant articles and documents

Preparation of synthetic auxin-amino acid conjugates

Revelou, Panagiota-Kyriaki,Constantinou-Kokotou, Violetta

, p. 1708 - 1712 (2019/05/15)

Auxin amide conjugates are regulators of the most important auxin, indole-3-acetic acid (IAA), which is considered responsible for many important processes within the plants. Herein, amide conjugates of IAA were synthesized employing a simple and efficient coupling method with WSCI·HCl, a water-soluble condensing reagent, in the presence of 1-hydroxybenzotriazole. IAA conjugates with 10 amino acids along with their corresponding methyl esters were prepared in excellent yields, up to 95%, aiming to facilitate their identification in plant species. Eight IAA-amino acid methyl ester conjugates are characterized here for the first time.

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