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4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID is a chemical compound with the molecular formula C6H8N2O2S, belonging to the thiazole family. It features a methylamino group, a carboxylic acid group, and a methyl group, which contribute to its diverse applications in various industries.

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  • 110859-69-3 Structure
  • Basic information

    1. Product Name: 4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID
    2. Synonyms: CHEMBRDG-BB 4010426;4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID;TIMTEC-BB SBB010541;4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylic acid;Albb-005441;4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylic acid(SALTDATA: 0.49H2O);5-Thiazolecarboxylic acid, 4-Methyl-2-(MethylaMino)-;4-methyl-2-methylamino-5-thiazolecarboxylic acid
    3. CAS NO:110859-69-3
    4. Molecular Formula: C6H8N2O2S
    5. Molecular Weight: 172.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 110859-69-3.mol
  • Chemical Properties

    1. Melting Point: 159-160 °C
    2. Boiling Point: 346.8°C at 760 mmHg
    3. Flash Point: 163.5°C
    4. Appearance: /
    5. Density: 1.43g/cm3
    6. Vapor Pressure: 2.13E-05mmHg at 25°C
    7. Refractive Index: 1.653
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 2.18±0.37(Predicted)
    11. CAS DataBase Reference: 4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID(110859-69-3)
    13. EPA Substance Registry System: 4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID(110859-69-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 110859-69-3(Hazardous Substances Data)

110859-69-3 Usage

Uses

Used in Pharmaceutical Industry:
4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID is used as an intermediate in the synthesis of drugs for various medical conditions. Its thiazole ring is known to exhibit biological activity, making it a promising candidate for the development of new pharmaceuticals.
Used in Agrochemical Industry:
In the agrochemical sector, 4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides. Its unique chemical structure allows for the development of effective and targeted agrochemicals.
Used in Chemical Industry for Materials Synthesis:
4-METHYL-2-METHYLAMINO-THIAZOLE-5-CARBOXYLIC ACID is employed as a key component in the synthesis of various materials in the chemical industry. Its versatile chemical properties enable the production of materials with specific characteristics, such as high thermal stability or unique electronic properties.
Overall, 4-Methyl-2-methylamino-thiazole-5-carboxylic acid is a versatile chemical with wide-ranging applications in research and industry, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 110859-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,5 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110859-69:
(8*1)+(7*1)+(6*0)+(5*8)+(4*5)+(3*9)+(2*6)+(1*9)=123
123 % 10 = 3
So 110859-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O2S/c1-3-4(5(9)10)11-6(7-2)8-3/h1-2H3,(H,7,8)(H,9,10)

110859-69-3 Well-known Company Product Price

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  • Aldrich

  • (CBR01089)  4-Methyl-2-(methylamino)-1,3-thiazole-5-carboxylic acid  AldrichCPR

  • 110859-69-3

  • CBR01089-1G

  • 1,159.47CNY

  • Detail

110859-69-3SDS

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 4-methyl-2-(methylamino)-1,3-thiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-methylamino-thiazole-5-carboxylic 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:110859-69-3 SDS

110859-69-3Downstream Products

110859-69-3Relevant articles and documents

Thiazolecarboxylic acid derivatives. 1. N-substituted 2-amino-4- methylthiazole-5-carboxylic acid derivatives

Dovlatyan,Eliazyan,Pivazyan,Kazaryan,Engoyan

, p. 84 - 89 (2004)

Acylation of the ethyl ester and anilide of 2-amino-4-methylthiazole-5- carboxylic acid gave 2-acetyl(arylsulfonyl)amino derivatives. Methylation of acetylaminothiazole and subsequent deacetylation gave 2-methylamino-4- methylthiazole-5-carboxylic acid, w

2-aminothiazolecarboxamide derivatives, processes for their preparation and their use for controlling phytopathogenic organisms

-

, (2008/06/13)

The present invention rlates to a novel 2-aminothiazolecarboxamide derivative represented by the following general formula (I) : in which R1 and R2independently of one another represent hydrogen, (C1-C5)alkyl, (C1-C5)haloalkyl, (C3-C6)alkenyl, (C3-C6)alkynyl, (C3-C6)cycloalkyl, or phenyl or benzyl, each of which can be substituted with halogen, (C1-C3)alkyl or nitro; R3represents (C1-C3)alkyl or (C1-C3)haloalkyl; R4represents 2-thienyl, 3-thienyl, 2-furyl, 3-furyl, phenyl, or phenyl or benzyl, each of which can be substituted with halogen, (C1-C6)alkyl or nitro; R5represents cyano or thiocarbamoyl; and R6represents (C1-C6)alkyl, (C3-C6)alkenyl, (C3-C6)cycloalkyl, or phenyl or benzyl, each of which can be substituted with halogen, (C1-C3)alkyl or nitro, which is a fungicidal agent useful for controlling phytopathogenic organisms. In addition, the present invention also relates to a process for preparing the novel 2-aminothiazolecarboxamide derivative of formula (I) and use of the compound of formula (I) as an agent for controlling phytopathogenic organisms.

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