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1H-Indole-3-acetic acid, 1-(2,3-dichlorobenzoyl)-5-methoxy-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

807614-98-8

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807614-98-8 Usage

Chemical class

Indole compounds

Natural occurrence

Commonly found in plants

Derivative of

1H-Indole-3-acetic acid (IAA)

Use in research

Tool to study the effects of IAA on plant growth and development

Modification

2,3-dichlorobenzoyl group and 5-methoxy-2-methyl group

Potential applications

Agriculture and biotechnology to influence plant growth and development

Check Digit Verification of cas no

The CAS Registry Mumber 807614-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,6,1 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 807614-98:
(8*8)+(7*0)+(6*7)+(5*6)+(4*1)+(3*4)+(2*9)+(1*8)=178
178 % 10 = 8
So 807614-98-8 is a valid CAS Registry Number.

807614-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1-(2,3-dichlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-acetic acid,1-(2,3-dichlorobenzoyl)-5-methoxy-2-methyl

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:807614-98-8 SDS

807614-98-8Upstream product

807614-98-8Downstream Products

807614-98-8Relevant academic research and scientific papers

Synthesis of COX-2 and FAAH inhibitors

-

, (2008/06/13)

Methods for preparing indoles that are useful COX-2 inhibitors and intermediates useful in such methods are described.

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