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BENZYL-(3-METHYL-ISOXAZOL-5-YLMETHYL)-AMINE is a versatile chemical compound characterized by the presence of a benzyl group connected to a 3-methyl-isoxazol-5-ylmethylamine group. It is widely recognized for its utility in organic synthesis, particularly as a fundamental building block in the creation of pharmaceutical and agrochemical compounds. BENZYL-(3-METHYL-ISOXAZOL-5-YLMETHYL)-AMINE's structural attributes and reactivity render it a promising candidate for the development of drugs and other bioactive substances, further establishing its significance as a key intermediate in the pharmaceutical sector.

154016-55-4

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154016-55-4 Usage

Uses

Used in Pharmaceutical Industry:
BENZYL-(3-METHYL-ISOXAZOL-5-YLMETHYL)-AMINE is used as a building block for the synthesis of various pharmaceutical compounds due to its ability to contribute to the development of drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, BENZYL-(3-METHYL-ISOXAZOL-5-YLMETHYL)-AMINE is utilized as a starting material for the preparation of agrochemicals, highlighting its role in the creation of compounds that can be employed in agricultural settings for pest control and crop protection.
Used in Organic Synthesis:
BENZYL-(3-METHYL-ISOXAZOL-5-YLMETHYL)-AMINE is used as a key intermediate in organic synthesis for the preparation of complex molecules with biological activity, underlining its importance in the synthesis of compounds that possess potential medicinal or biological significance.

Check Digit Verification of cas no

The CAS Registry Mumber 154016-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,1 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154016-55:
(8*1)+(7*5)+(6*4)+(5*0)+(4*1)+(3*6)+(2*5)+(1*5)=104
104 % 10 = 4
So 154016-55-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2O/c1-4-2-5(3-6)8-7-4/h2H,3,6H2,1H3

154016-55-4 Well-known Company Product Price

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  • Aldrich

  • (CBR00041)  1-(3-Methylisoxazol-5-yl)methanamine  AldrichCPR

  • 154016-55-4

  • CBR00041-1G

  • 4,512.69CNY

  • Detail

154016-55-4SDS

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 1-(3-Methylisoxazol-5-yl)methanamine

1.2 Other means of identification

Product number -
Other names (3-methyl-1,2-oxazol-5-yl)methanamine

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:154016-55-4 SDS

154016-55-4Relevant academic research and scientific papers

(3-HYDROXY-4-AMINO-BUTAN-2-YL) -3- (2-THIAZOL-2-YL-PYRROLIDINE-1-CARBONYL) BENZAMIDE DERIVATIVES AND RELATED COMPOUNDS AS BETA-SECRETASE INHIBITORS FOR TREATING

-

Page/Page column 87, (2009/05/29)

The present invention provides novel beta-secretase inhibitors and methods for their use, including methods of treating of Alzheimer's disease. (Formula)

GLYCYRRHETINIC ACID-30-AMIDE DERIVATIVES AND THE USES THEREOF

-

Page/Page column 10, (2008/12/06)

The present invention relates to the field of a medicine for treating diseases associated with inflammation, immunity or infection, and in particular, to glycyrrhetinic acid-30-amide derivatives of general formula I and their preparation, and a pharmaceutical composition containing the same. Said derivatives and composition exhibit anti -inflammatory, analgesic, anti-allergic, cough-preventing, liver-protecting and anti-viral properties, wherein each group is as defined in the description.

Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles: A facile and chemoselective reduction of azide to amino by sodium borohydride using 1,3-propanedithiol as a catalyst

Pei,Wickhan

, p. 7509 - 7512 (2007/10/02)

A series of isoxazole azides were reduced selectively to isoxazole amines in quantitative yield by sodium borohydride using 1,3-propanedithiol as a catalyst.

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