693-95-8 | 4-Methylthiazole

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$6.00	$5.00
25g	98%	in stock	$14.00	$10.00
100g	98%	in stock	$34.00	$24.00
500g	98%	in stock	$150.00	$105.00

Description

• Catalog Number: AB45102
• Chemical Name: 4-Methylthiazole
• CAS Number: 693-95-8
• Molecular Formula: C4H5NS
• Molecular Weight: 99.1542
• MDL Number: MFCD00005340
• SMILES: Cc1cscn1
• NSC Number: 42976

Computed Properties

• Complexity: 46.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 1

Upstream Synthesis Route

4-Methylthiazole is a versatile compound widely used in chemical synthesis for its unique properties and applications. This compound serves as an important building block in the creation of various pharmaceuticals, agrochemicals, and fragrance compounds. Its distinct structure and reactivity make it an essential component in the production of specialized chemicals and intermediates. Additionally, 4-Methylthiazole is utilized as a key ingredient in the formulation of flavor enhancers, giving products a characteristic savory or umami taste. Its presence in chemical synthesis processes plays a crucial role in achieving specific molecular structures and enhancing the overall functionality of the resulting compounds.

Literature

• Synthesis and pharmacological evaluation of a novel series of 3-aryl-2-(2-substituted-4-methylthiazole-5-yl)thiazolidin-4-one as possible anti-inflammatory and antimicrobial agents.

  Bioorganic & medicinal chemistry letters 20121015

• Design and synthesis of neuroprotective methylthiazoles and modification as NO-chimeras for neurodegenerative therapy.

  Journal of medicinal chemistry 20120809

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Anionic Fischer-type carbene complexes as bidentate (N,O) ligands.

  Dalton transactions (Cambridge, England : 2003) 20040421

• Method for determining nitrogenous heterocycle compounds in wine.

  Journal of agricultural and food chemistry 20021009

• Enzymatic assembly of epothilones: the EpoC subunit and reconstitution of the EpoA-ACP/B/C polyketide and nonribosomal peptide interfaces.

  Biochemistry 20020430

• Alternative heterocycles for DNA recognition: an N-methylpyrazole/N-methylpyrrole pair specifies for A.T/T.A base pairs.

  Bioorganic & medicinal chemistry 20010101