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6-acetaMido-1-oxo-2,3-dihydro-1H-indene-4-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

224181-99-1

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224181-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 224181-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,1,8 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 224181-99:
(8*2)+(7*2)+(6*4)+(5*1)+(4*8)+(3*1)+(2*9)+(1*9)=121
121 % 10 = 1
So 224181-99-1 is a valid CAS Registry Number.

224181-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-acetamido-1-oxo-2,3-dihydroindene-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-acetylamino-1-oxo-indan-4-carboxylic acid

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:224181-99-1 SDS

224181-99-1Downstream Products

224181-99-1Relevant academic research and scientific papers

Synthesis of 6-azido-1-oxo-indan-4-oyl isoleucine; a photoaffinity approach to plant signaling

Schueler, Goede,Wasternack, Claus,Boland, Wilhelm

, p. 3897 - 3904 (2007/10/03)

The synthesis of the photoreactive 6-azido-1-oxo-indanoyl isoleucine (3), as a molecular probe for the identification of putative receptors and binding proteins involved in stress signaling of plants, is described. The biological activity of the photolabile azide 3 comes close to that of the bacterial phytotoxin coronatine (1). Photodecomposition of 3 in the presence of myoglobin is assumed to proceed via an didehydroazepine intermediate and results in significant binding of the probe to the model protein.

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