1003-61-8

Basic information

• Product Name: 2-Amino-5-formylthiazole
• Synonyms: 2-AMINOTHIAZOLE-5-CARBALDEHYDE;2-AMINOTHIAZOLE-5-CARBOXALDEHYDE;2-AMINO-5-FORMYLTHIAZOLE;2-Amino-5-formyl-1,3-thiazole;2-Aminothiazole-5-carbadehyde;2-Amino-1,3-thiazole-5-carboxaldehyde 96%;2-AMINOTHIAZOLE-5-CARBALDEHYDE, 98+%;2-AMINOTHIAZOLE-5-CARBALDEHYDE 95%
• CAS NO: 1003-61-8
• Molecular Formula: C₄H₄N₂OS
• Molecular Weight: 128.15
• Product Categories: Aldehydes;Amines;blocks;Thiazoles;Sulphur Derivatives;Thiazoles, Isothiazoles &Benzothiazoles;Thiazole;Thiazoles, Isothiazoles & Benzothiazoles;Building Blocks
• Mol File: 1003-61-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 122-132 °C
• Boiling Point: 316.3 °C at 760 mmHg
• Flash Point: 145.1 °C
• Appearance: /
• Density: 1.488 g/cm³
• Vapor Pressure: 0.000413mmHg at 25°C
• Refractive Index: 1.712
• Storage Temp.: Keep Cold
• PKA: 3.16±0.10(Predicted)
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2-Amino-5-formylthiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Amino-5-formylthiazole(1003-61-8)
• EPA Substance Registry System: 2-Amino-5-formylthiazole(1003-61-8)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 22-36/37/38-43
• Safety Statements: 26-36/37
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 1003-61-8(Hazardous Substances Data)

Usage

Chemical Properties

Solid

Uses

Different sources of media describe the Uses of 1003-61-8 differently. You can refer to the following data:
1. The presence of different functional groups allows differential attachment of an azo linkage and benzoxazolium salt providing cationic, delocalized azo dyes.
2. 2-Amino-5-formylthiazole is a useful reagent for the preparation of cationic azo dyes.

InChI:InChI=1/C4H4N2OS/c5-4-6-1-3(2-7)8-4/h1-2H,(H2,5,6)

Upstream product

• 32284-60-9 N,N-bis(trimethylsilyl)-2-aminothiazole 
• 68-12-2 N,N-dimethyl-formamide 
• 2065-75-0 2-Bromo-malonaldehyde 
• 17356-08-0 thiourea 

Downstream Products

• 1005-28-3 2-(dimethylamino)thiazole-5-carbaldehyde 
• 1253116-34-5 C₁₁H₁₅N₃O₂S 
• 252662-37-6 N-(5-formyl-1,3-thiazol-2-yl)acetamide 
• 320423-50-5 2-(4-methylpiperazin-1-yl)thiazole-5-carboxaldehyde 
• 1228304-57-1 6-(4-chlorophenyl)imidazo[2,1-b][1,3]thiazole-2-carbaldehyde 
• 924668-30-4 C₁₂H₇F₄N₃O₂S 
• 936845-87-3 4-[4-(5-formyl-thiazol-2-ylamino)-benzenesulfonyl]-piperidine-1-carboxylic acid tert-butyl ester 
• 936845-85-1 4-[6-(5-formyl-thiazol-2-ylamino)-2-methyl-pyrimidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester 
• 859523-71-0 1,1-dicyclohexyl-3-(5-formyl-thiazol-2-yl)-urea 
• 464192-28-7 2-bromo-1,3-thiazole-5-carbaldehyde 
• 391668-77-2 tert-butyl (5-formylthiazol-2-yl)carbamate 
• 1001419-48-2 C₁₉H₂₂N₂O₄S₂ 
• 131184-73-1 (2-amino-1,3-thiazol-5-yl)methanol 

Relevant articles and documents

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SUBSTITUTED QUINAZOLINE DERIVATIVES AND THEIR USE AS INHIBITORS

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Process for preparing 2-amino-5-formylthiazole and its hydrobromide salt

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