1004-00-8 | 2-Amino-4-chlorothiophenol

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$5.00	$4.00
5g	96%	in stock	$7.00	$5.00
10g	96%	in stock	$14.00	$10.00
25g	96%	in stock	$20.00	$14.00

Description

• Catalog Number: AA02265
• Chemical Name: 2-Amino-4-chlorothiophenol
• CAS Number: 1004-00-8
• Molecular Formula: C6H6ClNS
• Molecular Weight: 159.63654000000002
• MDL Number: MFCD00792528
• SMILES: Clc1ccc(c(c1)N)S

Computed Properties

• Complexity: 99.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• XLogP3: 2.4

Upstream Synthesis Route

2-Amino-4-chlorobenzenethiol, also known as ACBT, is a versatile chemical compound frequently utilized in organic synthesis. With its unique structure and reactivity, ACBT plays a crucial role in various chemical reactions and processes, making it an essential building block in the field of chemistry.One of the key applications of 2-Amino-4-chlorobenzenethiol in chemical synthesis is its use as a precursor in the production of dyes and pigments. By reacting ACBT with other chemicals or compounds, chemists can create vibrant and stable colorants that are used in a wide range of industries, including textiles, paints, and plastics.Additionally, ACBT is often employed in the synthesis of pharmaceuticals and agrochemicals. Its ability to undergo various transformations and form complex molecular structures makes it a valuable starting material in the development of new drugs, pesticides, and other biologically active compounds.Moreover, 2-Amino-4-chlorobenzenethiol serves as a vital reagent in the construction of organic molecules with sulfur-containing functional groups. Its sulfur atom can participate in multiple types of reactions, such as thiol-disulfide exchange and nucleophilic substitution, allowing for the creation of diverse sulfur-based compounds with tailored properties.In summary, the significance of 2-Amino-4-chlorobenzenethiol in chemical synthesis lies in its versatility and reactivity, enabling its widespread use as a fundamental building block for the creation of dyes, pharmaceuticals, agrochemicals, and sulfur-containing organic molecules.

Literature

• 5-Chloro-4'-ethyl-3H-spiro-[1,3-benzo-thia-zole-2,1'-cyclo-hexa-ne].

  Acta crystallographica. Section E, Structure reports online 20120501

• 4'-tert-Butyl-5-chloro-3H-spiro-[1,3-benzothia-zole-2,1'-cyclo-hexa-ne].

  Acta crystallographica. Section E, Structure reports online 20120501