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1H-Indole-1-acetic acid, 5-[3-[(6-benzoyl-1-propyl-2-naphthalenyl)oxy]propoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853652-40-1

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853652-40-1 Usage

Molecular structure

The compound has a complex structure that includes an indole ring, a naphthalene ring, a benzoyl group, and a propoxy chain.

Type of compound

It is a derivative of 1H-Indole-1-acetic acid, which is a plant hormone known as auxin.

Biological activity

The compound likely has biological activity similar to that of indole-3-acetic acid, which plays a role in plant growth and development.

Research and biotechnology applications

The compound may be used in research and biotechnology applications related to plant growth and development.

Context-dependent structure and functions

The specific structure and functions of the compound will depend on the context in which it is studied and used.

Check Digit Verification of cas no

The CAS Registry Mumber 853652-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,6,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 853652-40:
(8*8)+(7*5)+(6*3)+(5*6)+(4*5)+(3*2)+(2*4)+(1*0)=181
181 % 10 = 1
So 853652-40-1 is a valid CAS Registry Number.

853652-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-{3-[(6-Benzoyl-1-propyl-2-naphthyl)oxy]propoxy}-1H-indol-1-yl) acetic acid

1.2 Other means of identification

Product number -
Other names -

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:853652-40-1 SDS

853652-40-1Downstream Products

853652-40-1Relevant academic research and scientific papers

Indol-1-yl acetic acids as peroxisome proliferator-activated receptor agonists: Design, synthesis, structural biology, and molecular docking studies

Mahindroo, Neeraj,Wang, Chiung-Chiu,Liao, Chun-Chen,Huang, Chien-Fu,Lu, I.-Lin,Lien, Tzu-Wen,Peng, Yi-Huei,Huang, Wei-Jan,Lin, Ying-Ting,Hsu, Ming-Chen,Lin, Chia-Hui,Tsai, Chia-Hua,Hsu, John T.-A.,Chen, Xin,Lyu, Ping-Chiang,Chao, Yu-Sheng,Wu, Su-Ying,Hsieh, Hsing-Pang

, p. 1212 - 1216 (2007/10/03)

A series of novel indole-based PPAR agonists is described leading to discovery of 10k, a highly potent PPAR pan-agonist. The structural biology and molecular docking studies revealed that the distances between the acidic group and the linker, when a ligan

Indole compounds

-

Page/Page column 49, (2008/06/13)

This invention relates to treating peroxisome proliferator-activated receptors related diseases with certain indole compounds. The indole compounds are of formula (I) below. Each variable is defined in the specification.

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