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3,3-bis(1-ethyl-2-methyl-1H-indol-3-yl)phthalide is a complex chemical compound derived from phthalide, characterized by its unique molecular structure featuring two indole groups attached to the phthalide core, each substituted with ethyl and methyl groups. This distinctive arrangement endows the compound with specific properties that make it a candidate for various applications across different industries.

22091-92-5

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22091-92-5 Usage

Uses

Used in Pharmaceutical Industry:
3,3-bis(1-ethyl-2-methyl-1H-indol-3-yl)phthalide is used as a potential pharmaceutical agent for its unique molecular interactions and properties that may contribute to the development of new drugs or therapeutic agents. Its specific application reason in this industry would require further research and testing to determine its efficacy and safety.
Used in Agrochemical Industry:
In the agrochemical sector, 3,3-bis(1-ethyl-2-methyl-1H-indol-3-yl)phthalide is utilized as a component in the development of new agrochemicals, potentially offering novel modes of action for pest control or crop protection. The application reason here is based on its chemical structure that may provide innovative solutions to agricultural challenges.
Used in Materials Science:
3,3-bis(1-ethyl-2-methyl-1H-indol-3-yl)phthalide is employed in materials science for its potential to contribute to the creation of new materials with unique properties. Its application reason in this field is due to the possibility of its structural features influencing material characteristics such as stability, reactivity, or other physical and chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 22091-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22091-92:
(7*2)+(6*2)+(5*0)+(4*9)+(3*1)+(2*9)+(1*2)=85
85 % 10 = 5
So 22091-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C30H28N2O2/c1-5-31-19(3)27(22-14-8-11-17-25(22)31)30(24-16-10-7-13-21(24)29(33)34-30)28-20(4)32(6-2)26-18-12-9-15-23(26)28/h7-18H,5-6H2,1-4H3

22091-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-bis(1-ethyl-2-methylindol-3-yl)-phthalide

1.2 Other means of identification

Product number -
Other names N,N'-diethyl-α-skatolephthalein

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:22091-92-5 SDS

22091-92-5Upstream product

22091-92-5Downstream Products

22091-92-5Relevant academic research and scientific papers

Salicylic acid derivatives

-

, (2008/06/13)

The heat-sensitive recording material disclosed comprises a colorless or pale colored dyestuff precursor, one or more salicylic acid derivative of the formula (1) or metal salt of the derivative and an aliphatic amide compound having 18?60 carbon atoms in molecular structure, and is excellent in thermal response and preservation stability of white portions and images. STR1 wherein X1 and X2 are a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an aralkyl group or an aryl group, Y1 and Y2 are an oxygen atom or a sulfur atom, R1 is a hydrogen atom, an alkyl group, an aralkyl group or an aryl group, and R2 is an alkyl group, an alkenyl group, an aralkyl group or an aryl group.

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