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113772-14-8

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113772-14-8 Usage

Description

1H-Indole-3-carboxylicacid,2-amino-,methylester(9CI), also known as Methyl 2-aminoindole-3-carboxylate, is an organic compound with the chemical formula C10H10N2O2. It is a derivative of indole-3-carboxylic acid, featuring an amino group at the 2nd position and a methyl ester group at the 3rd position. 1H-Indole-3-carboxylicacid,2-amino-,methylester(9CI) is characterized by its unique structure and properties, making it a valuable intermediate in organic synthesis.

Uses

Used in Organic Synthesis:
1H-Indole-3-carboxylicacid,2-amino-,methylester(9CI) is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for the formation of a wide range of derivatives, which can be further utilized in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1H-Indole-3-carboxylicacid,2-amino-,methylester(9CI) serves as a key building block for the development of novel drug candidates. Its versatile chemical properties enable the design and synthesis of new molecules with potential therapeutic applications, such as anti-inflammatory, analgesic, and anti-cancer agents.
Used in Agrochemical Industry:
1H-Indole-3-carboxylicacid,2-amino-,methylester(9CI) is also employed in the agrochemical industry for the synthesis of bioactive compounds with pesticidal properties. Its ability to form various derivatives makes it a valuable precursor for the development of new pesticides and plant growth regulators.

Check Digit Verification of cas no

The CAS Registry Mumber 113772-14-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,7 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113772-14:
(8*1)+(7*1)+(6*3)+(5*7)+(4*7)+(3*2)+(2*1)+(1*4)=108
108 % 10 = 8
So 113772-14-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c1-14-10(13)8-6-4-2-3-5-7(6)12-9(8)11/h2-5,12H,11H2,1H3

113772-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-amino-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Aminoindole-3-carboxylic Acid Methyl Ester

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:113772-14-8 SDS

113772-14-8Relevant articles and documents

Method for preparing 2-aminoindole derivative

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Paragraph 0031, (2018/09/12)

The invention discloses a method for preparing a 2-aminoindole derivative. The method provided by the invention has the following advantages: pyridine formylindole is used as a starting material, so raw materials are easily-available and have extensive varieties; products obtained by the utilizing the method provided by the invention have various types and extensive use, and can be directly used and can be used for synthesis of drugs; in addition, the method disclosed by the invention has the advantages of simple steps, mild reaction conditions, high target product yield, less pollution, simple reaction operation and post-treatment process, and applicability to industrial production.

COMPOUNDS AND METHODS

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, (2011/06/11)

Disclosed are compounds having formula (I), wherein R1, R2, R3, R4, Z1, Z2, Z3 and Z4 are as defined herein, and methods of making and using the same.

Syntheses of Functionalised Pyridoindoles

Forbes, Ian T.,Johnson, Christopher N.,Thompson, Mervyn

, p. 275 - 282 (2007/10/02)

Two complementary routes for the synthesis of highly functionalised pyridoindoles are described, starting from the readily available 2-amino-3-cyano-1-(4-methoxybenzyl)tetrahydroindole and methyl 2-aminoindole-3-carboxylate, respectively.The use of

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