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2-Methyl-2,3-dihydrobenzofuran-7-aMine, with the molecular formula C11H13NO, is an amine derivative of 2-methyl-2,3-dihydrobenzofuran. It features a benzofuran backbone with a methyl substitution at the 2-position and an amine group at the 7-position. This chemical compound is widely used in the synthesis of pharmaceuticals and agrochemicals, serving as a versatile building block in organic synthesis. Its unique structure and properties also make it a promising target for research and development in medicinal chemistry, drug discovery, and organic chemistry.

26210-74-2

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26210-74-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Methyl-2,3-dihydrobenzofuran-7-aMine is used as an intermediate in the synthesis of various pharmaceuticals for its potential therapeutic applications. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Methyl-2,3-dihydrobenzofuran-7-aMine is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective compounds for crop protection and management.
Used in Medicinal Chemistry Research:
2-Methyl-2,3-dihydrobenzofuran-7-aMine is employed as a key building block in medicinal chemistry research, facilitating the design and synthesis of novel bioactive molecules. Its unique structure and reactivity contribute to the discovery of new drug candidates with potential therapeutic benefits.
Used in Drug Discovery:
As a component in drug discovery processes, 2-Methyl-2,3-dihydrobenzofuran-7-aMine aids in the identification and optimization of lead compounds. Its versatile chemical properties enable the exploration of various chemical space, leading to the development of innovative therapeutic agents.
Used in Organic Chemistry Research and Development:
2-Methyl-2,3-dihydrobenzofuran-7-aMine is an interesting target for research and development in the field of organic chemistry. Its unique structure and properties provide opportunities for the investigation of novel synthetic methods, reaction mechanisms, and the exploration of its potential applications in various chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 26210-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26210-74:
(7*2)+(6*6)+(5*2)+(4*1)+(3*0)+(2*7)+(1*4)=82
82 % 10 = 2
So 26210-74-2 is a valid CAS Registry Number.

26210-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-amino-2-methylcoumaran

1.2 Other means of identification

Product number -
Other names 2-methyl-2,3-dihydrobenzofuran-7-amine

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:26210-74-2 SDS

26210-74-2Downstream Products

26210-74-2Relevant academic research and scientific papers

SYNTHESIS OF AMINO-SUBSTITUTED 2-METHYLCOUMARINS, CHROMANS, AND BENZOXEPANES AND THEIR N-(ALKYLAMINOACYL) DERIVATIVES

Daukshas, V. K.,Pyatrauskas, O. Yu.,Purvanyatskas, G. N.

, p. 266 - 270 (2007/10/02)

The isomeric compositions of the products of nitration of 2-methylcoumaran and chroman with acetyl nitrate were determined.More convenient methods for the synhtesis of 7-amino-2-methylcoumaran and 8-aminochroman were developed, and 9-amino-1-benzoxepane was obtained for the first time.Alkylaminoacylaminosubstituted 2-methylcoumarans, chromans, and 1-benzoxepanes were synthesized.A method for the synthesis of 2-bromocaproyl chloride from caproic acid was developed.

Miticidal 2-(2-alkyl-2,3-dihydrobenzofuran-7-yl)-N-alkoxy-N-alkyl-diazenecarboxamides

-

, (2008/06/13)

Miticidal 2-(2-alkyl-4-(or 5)-bromo (or chloro)-2,3-dihydrobenzofuran-7-yl)-N-alkoxy-N-alkyldiazenecarboxamides.

Aphicidal 3-(2-alkyl-2,3-dihydrobenzofuran-7-yl)-5-(R,R1 -amino)-1,3,4-oxadiazol-2(3H)-ones

-

, (2008/06/13)

Certain aphicidal 3-(2-alkyl-2,3-dihydrobenzofuran-7-yl)-5-(R,R1 -amino)-1,3,4-oxadiazol-2(3H)-ones.

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