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(4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE, with the chemical formula C5H10N2S, is a derivative of thiazole, a five-membered heterocyclic compound that includes a sulfur atom and an additional nitrogen atom. (4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE is recognized for its versatility in organic synthesis and potential biological activity.

51221-45-5

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51221-45-5 Usage

Uses

Used in Pharmaceutical Synthesis:
(4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with diverse therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, (4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE is utilized as a component in the creation of various agrochemicals, potentially enhancing crop protection and yield.
Used in Dye Manufacturing:
(4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE is employed as a key intermediate in the production of dyes, contributing to the colorfastness and vibrancy of textiles and other materials.
Used in Chemical Research:
As a reagent in chemical research, (4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE aids in the exploration of new chemical reactions and the discovery of novel compounds.
Used in Drug Discovery:
(4-METHYL-1,3-THIAZOL-2-YL)METHYLAMINE is used in drug discovery processes to identify potential therapeutic agents, capitalizing on its antimicrobial and antifungal properties for medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 51221-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,2 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51221-45:
(7*5)+(6*1)+(5*2)+(4*2)+(3*1)+(2*4)+(1*5)=75
75 % 10 = 5
So 51221-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2S/c1-4-3-8-5(2-6)7-4/h3H,2,6H2,1H3

51221-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methyl-1,3-thiazol-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names (4-methyl-1,3-thiazol-2-yl)methylamine

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:51221-45-5 SDS

51221-45-5Relevant academic research and scientific papers

OXADIAZOLE COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

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Page/Page column 81-82, (2012/05/05)

The invention provides novel beta-secretase inhibitors and methods for their including methods of treating Alzheimer's disease.

COMPOUNDS CONTAINING FUSED RINGS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

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Page/Page column 80, (2011/11/01)

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

COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

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Page/Page column 75, (2009/03/07)

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

(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

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Page/Page column 65, (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)

COMPOUNDS WHICH INHIBIT BETA-SECRETASE ACTIVITY AND METHODS OF USE THEREOF

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Page/Page column 49-50, (2008/06/13)

The present invention provides novel beta-secretase inhibitors of the general formula (I), where the variables A1, A2, L1, L2, L3, R1, R2, R3, R4, R5, R6 and R7 are as defined in the claims, a method for their use in treating Alzheimer's disease, and methods for their use in reducing memapsin 2 catalytic activity.

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