1226056-71-8 | Thiazovivin

Packsize	Purity	Availability	Price	Discounted Price
1mg	98%	in stock	$29.00	$20.00
5mg	98%	in stock	$43.00	$30.00
10mg	98%	in stock	$55.00	$38.00
100mg	98%	in stock	$117.00	$82.00
250mg	98%	in stock	$223.00	$156.00
1g	98%	in stock	$554.00	$388.00

Description

• Catalog Number: AA56226
• Chemical Name: Thiazovivin
• CAS Number: 1226056-71-8
• Molecular Formula: C15H13N5OS
• Molecular Weight: 311.3616
• MDL Number: MFCD16495823
• SMILES: O=C(c1csc(n1)Nc1ccncn1)NCc1ccccc1

Computed Properties

• Complexity: 364
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 2.5

Upstream Synthesis Route

N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide is a versatile compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules due to its functional groups and reactivity. In particular, its structure containing a thiazole ring, pyrimidine moiety, and an amide group provides a platform for forming complex structures through selective chemical reactions. The presence of the phenylmethyl group adds further diversity to its chemical reactivity, allowing for modifications and derivatization to tailor its properties for specific applications. In chemical synthesis, N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide can be utilized as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials with desired properties. Its ability to participate in various coupling reactions, functional group transformations, and cyclization processes makes it a valuable tool for organic chemists seeking to construct intricate molecular frameworks efficiently. This compound's role in chemical synthesis extends beyond mere intermediacy, as its structural motifs can confer important biological activities or physical characteristics to final products. By harnessing the chemical versatility of N-(Phenylmethyl)-2-(4-pyrimidinylamino)-4-thiazolecarboxamide, researchers can access new pathways for synthesizing diverse compounds with potential applications in various industries.

Literature

• Resveratrol prevents AngII-induced hypertension via AMPK activation and RhoA/ROCK suppression in mice.

  Hypertension research : official journal of the Japanese Society of Hypertension 20140901

• Direct conversion of porcine embryonic fibroblasts into adipocytes by chemical molecules.

  Cellular reprogramming 20120401

• A chemical platform for improved induction of human iPSCs.

  Nature methods 20091101