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(3-FORMYL-2-METHYL-INDOL-1-YL)-ACETIC ACID is an organic compound with a complex chemical structure, characterized by a formyl group at the 3rd position, a methyl group at the 2nd position, and an indole ring attached to an acetic acid moiety. This molecule is known for its potential applications in the pharmaceutical and chemical industries due to its unique properties and reactivity.

432001-45-1

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432001-45-1 Usage

Uses

Used in Pharmaceutical Industry:
(3-FORMYL-2-METHYL-INDOL-1-YL)-ACETIC ACID is used as a reagent for the preparation of heterocyclic compounds acting as tyrosine kinase modulators. These modulators play a crucial role in the development of targeted therapies for various diseases, including cancer, by regulating the activity of tyrosine kinase enzymes.
Used in Chemical Synthesis:
(3-FORMYL-2-METHYL-INDOL-1-YL)-ACETIC ACID is also used as a building block in the synthesis of various complex organic molecules, particularly those with potential applications in the pharmaceutical, agrochemical, and materials science industries. Its unique structure and reactivity make it a valuable component in the development of new drugs, agrochemicals, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 432001-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,0,0 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 432001-45:
(8*4)+(7*3)+(6*2)+(5*0)+(4*0)+(3*1)+(2*4)+(1*5)=81
81 % 10 = 1
So 432001-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3/c1-8-10(7-14)9-4-2-3-5-11(9)13(8)6-12(15)16/h2-5,7H,6H2,1H3,(H,15,16)

432001-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Formyl-2-methyl-indol-1-yl)-acetic acid

1.2 Other means of identification

Product number -
Other names 2-(3-formyl-2-methylindol-1-yl)acetic 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:432001-45-1 SDS

432001-45-1Downstream Products

432001-45-1Relevant academic research and scientific papers

Indanediones-1,3 VIII. Hydroxy-2 indolyl-2 indanediones-1,3, (indolyl-3 methylene)-2 indanediones-1,3 et derives: recherche d'une activite anti-inflammatoire

Courant, Jacqueline,Leblois, Danielle,Tandon, Manju,Robert-Piessard, Sylvie,le Baut, Guillaume,et al.

, p. 145 - 154 (2007/10/02)

1,3-Indandiones VIII. 2-Hydroxy-2-indolyl-1,3-indandiones, 2-(indol-3-ylmethylene indandione and derivatives: search for anti-inflammatory activity.A series of 2-hydroxy-2-indolyl-1,3-indandiones, diversely substituted on the heterocycle were synthetized in order to study their anti-inflammatory activity.Catalytic hydrogenation gave 2,3-dihydroxy-1 indanones 6 and NaBH4 reduction of 3i led to the corresponding indanetriol 7i.Base-catalyzed isomerization of hydroxy-β-diketones 3 furnished 3-indololylcarbonyl phthalides 9.Only compound 3d exhibited a significant inhibition of mouse paw edema.Experimentation in the rat paw edema test confirmed the anti-inflammatory effect of 3d, but it was associated with an anti-coagulant activity. ω-Amino-alkylation of the indole nitrogen of 3d led to loss of anti-inflammatory activity.Introduction of a double bond between the indandione and indole nuclei, leading to 2-(indol-3-ylmethylene)-1,3 indandiones 12, proved ineffective in raising this activity. 2-hydroxy-2-indolyl-1,3-indandiones/ 2,3-dihydroxyindanones/ 1,2,3-indantriols/ 3-indolylcarbonyl-phthalides/ 2-(indol-3-ylmethylene)-1,3-indandiones/ anti-inflammatory activity/ anti-coagulant activity

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