25475-76-7 | Thiophen-3-amine hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$7.00	$5.00
5g	98%	in stock	$31.00	$22.00
10g	98%	in stock	$56.00	$40.00
25g	98%	in stock	$120.00	$84.00

Description

• Catalog Number: AF32745
• Chemical Name: Thiophen-3-amine hydrochloride
• CAS Number: 25475-76-7
• Molecular Formula: C4H6ClNS
• Molecular Weight: 135.6151
• MDL Number: MFCD11226843
• SMILES: Nc1cscc1.Cl

Computed Properties

• Complexity: 46.8
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2

Upstream Synthesis Route

Thiophen-3-amine hydrochloride, also known as 3-aminothiophene hydrochloride, is a versatile chemical compound widely used in various chemical synthesis processes. Its application in organic synthesis is particularly notable due to its unique properties and reactivity.In chemical synthesis, Thiophen-3-amine hydrochloride can serve as a valuable building block for the construction of various heterocyclic compounds. Its amine functional group allows for straightforward derivatization, enabling the introduction of different substituents or linkers to tailor the molecule's properties. This versatility makes it a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, Thiophen-3-amine hydrochloride can participate in a range of important reactions, including nucleophilic substitution, reductive amination, and cross-coupling reactions. Its thienyl moiety provides unique electronic properties that can influence the reactivity and selectivity of the overall transformation. This makes it a valuable tool for organic chemists seeking to design and synthesize complex molecules with specific functionalities.Overall, Thiophen-3-amine hydrochloride plays a crucial role in modern chemical synthesis by offering synthetic chemists a versatile and reliable building block for the creation of diverse and valuable compounds. Its applications extend across various industries, highlighting its importance in the field of organic chemistry.