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2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88433-15-2

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88433-15-2 Usage

Indole Derivative

2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol belongs to the class of indole derivatives, which are compounds that are modified versions of the indole ring.

Ethanol Derivative

2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol is an ethanol derivative, meaning that it contains a hydroxyl group (-OH) attached to an ethyl group (-CH2-CH3).

Pharmaceutical Building Block

2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol is commonly used in the pharmaceutical industry as a building block in the synthesis of various drugs.

Organic Chemistry and Materials Science Applications

2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol may have potential applications in the field of organic chemistry and materials science.

Indole Ring

The structure of 2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol contains an indole ring, which is a common structural motif found in many biologically active compounds.

Important Intermediate

2-(2-ethoxy-3-methyl-3H-indol-3-yl)ethanol is an important intermediate in the development of novel pharmaceuticals due to its indole ring structure and its use as a building block in drug synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 88433-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,3 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88433-15:
(7*8)+(6*8)+(5*4)+(4*3)+(3*3)+(2*1)+(1*5)=152
152 % 10 = 2
So 88433-15-2 is a valid CAS Registry Number.

88433-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-ethoxy-3-methylindol-3-yl)ethanol

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:88433-15-2 SDS

88433-15-2Downstream Products

88433-15-2Relevant academic research and scientific papers

Reactions of 2-Hydroxytryptophol: Results of Strong Acid and Alkaline Treatments of 2-Hydroxytryptophol

Nozoye, Toshikazu,Shibanuma, Yoshihisa,Nakai, Tatsuya

, p. 2986 - 2992 (2007/10/02)

Upon being warmed at 90 deg C in trifluoromethanesulfonic acid for 42-78 h, 2-hydroxytriptophol (4a) gave 3-ethylideneoxidoles (E- and Z-form) (5a), while 3-methyl- (4b) or 3-ethyl-2-hydroxytryptophol (4c) gave the corresponding 3-alkylideneoxindoles (5b,

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