593-71-5 | Chloroiodomethane

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$34.00	$24.00
100g	97% stabilized with Copper chip	in stock	$46.00	$33.00
500g	97% stabilized with Copper chip	in stock	$170.00	$119.00

Description

• Catalog Number: AB71948
• Chemical Name: Chloroiodomethane
• CAS Number: 593-71-5
• Molecular Formula: CH2ClI
• Molecular Weight: 176.3841
• MDL Number: MFCD00001078
• SMILES: ClCI

Computed Properties

• Complexity: 4.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.6

Upstream Synthesis Route

Chloroiodomethane is a versatile chemical compound commonly used in organic synthesis due to its unique properties and reactivity. As a halomethane derivative, Chloroiodomethane serves as an important building block in the preparation of various organic compounds. Its selective chlorination and iodination reactions make it valuable in the creation of complex molecules with specific substitution patterns.In chemical synthesis, Chloroiodomethane is frequently employed as a chlorinating and iodinating agent in various reactions. It can efficiently introduce chlorine and iodine functionalities into organic molecules, allowing chemists to modify the structure and properties of the target compounds. Additionally, Chloroiodomethane's reactivity under different reaction conditions makes it a versatile tool for synthesizing pharmaceuticals, agrochemicals, and fine chemicals.Furthermore, Chloroiodomethane plays a crucial role in the preparation of advanced materials, such as polymers, specialty chemicals, and biologically active compounds. Its ability to facilitate selective halogenation reactions enables chemists to control the regioselectivity and stereoselectivity of the synthetic pathways, leading to the production of high-quality products with specific chemical properties.Overall, Chloroiodomethane's utility in chemical synthesis stems from its selective chlorination and iodination capabilities, making it a valuable reagent for the creation of diverse organic compounds in various industries.

Literature

• Formation and relaxation dynamics of iso-CH2Cl-I in cryogenic matrices.

  The Journal of chemical physics 20110921

• Addition reactions of chloro- or iodomethyllithium to imines. Synthesis of enantiopure aziridines and beta-chloroamines.

  The Journal of organic chemistry 20090320

• A 193 nm laser photofragmentation time-of-flight mass spectrometric study of chloroiodomethane.

  The Journal of chemical physics 20051101

• A dramatic spin-orbit effect observed in the vibrational frequencies of the chloroiodomethane cation.

  Angewandte Chemie (International ed. in English) 20050506

• Isolation of iodide-oxidizing bacteria from iodide-rich natural gas brines and seawaters.

  Microbial ecology 20050501