Isothiazole
- Product Name
- Isothiazole
- CAS No.
- 288-16-4
- Chemical Name
- Isothiazole
- Synonyms
- EOS-61208;1,2-Thiazol;Isothiazole;1,2-thiazole;2-Azathiophene;Isothiazole>288-16-4 Isothiazole;Isothiazole (6CI, 7CI, 8CI, 9CI, ACI)
- CBNumber
- CB91074072
- Molecular Formula
- C3H3NS
- Formula Weight
- 85.13
- MOL File
- 288-16-4.mol
Isothiazole Property
- Melting point:
- 176 °C (decomp)(Solv: water (7732-18-5))
- Boiling point:
- 114°C(lit.)
- Density
- 1.1566 (rough estimate)
- refractive index
- 1.5280 to 1.5320
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- Chloroform, Ethyl Acetate
- form
- Oil
- pka
- 4.00±0.12(Predicted)
- color
- Clear Colourless
- λmax
- 242nm(lit.)
Safety
- RIDADR
- UN 1993 3/PG II
- HS Code
- 2934.10.2000
- HazardClass
- 3
- PackingGroup
- II
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H225Highly Flammable liquid and vapour
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233Keep container tightly closed.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242Use only non-sparking tools.
P243Take precautionary measures against static discharge.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P321Specific treatment (see … on this label).
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P362Take off contaminated clothing and wash before reuse.
P370+P378In case of fire: Use … for extinction.
P403+P235Store in a well-ventilated place. Keep cool.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- I0982
- Product name
- Isothiazole
- Purity
- >98.0%(GC)
- Packaging
- 200mg
- Price
- $50
- Updated
- 2024/03/01
- Product number
- I0982
- Product name
- Isothiazole
- Purity
- >98.0%(GC)
- Packaging
- 1g
- Price
- $147
- Updated
- 2024/03/01
- Product number
- I917605
- Product name
- Isothiazole
- Packaging
- 500mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- 133212
- Product name
- Isothiazole
- Purity
- 97%
- Packaging
- 10g
- Price
- $1296
- Updated
- 2021/12/16
- Product number
- 65704
- Product name
- Isothiazole
- Packaging
- 5G
- Price
- $2000
- Updated
- 2021/12/16
Isothiazole Chemical Properties,Usage,Production
Chemical Properties
Isothiazole is a colorless liquid with a pyridine-like odor. It is only slightly soluble in water but readily dissolves in organic solvents such as ethanol and benzene. When treated with butyl lithium at -70°C, it undergoes lithiation at the 5-position. Isothiazole serves as a versatile intermediate for the synthesis of various 5-substituted derivatives, including alkyl groups (R-), formyl (-CHO), carboxyl (-COOH), and acyl groups (RCO-), among others. Electrophilic substitution reactions, such as nitration, sulfonation, and halogenation, predominantly occur at the 4-position.
Uses
Isothiazole, is a versatile building block that can be used in the synthesis of more complex compounds with biological activity such as the pharmaceutical drugs ziprasidone (Z485000), and perospirone (P288900).
Definition
ChEBI: Isothiazole is a mancude organic heteromonocyclic parent, a monocyclic heteroarene and a member of 1,2-thiazoles.
Preparation
Isothiazole can be prepared by the reaction of propiolic aldehyde with sodium thiocyanate to first produce 3-thiocyanatoacrolein (NCSCH=CHCHO), which is then reacted with ammonia to obtain isothiazole.
References
[1] LAI CHEN. Discovery of Novel Isothiazole, 1,2,3-Thiadiazole, and Thiazole-Based Cinnamamides as Fungicidal Candidates[J]. Journal of Agricultural and Food Chemistry, 2019, 67 45: 12357-12365. DOI:10.1021/acs.jafc.9b03891.
[2] A. KLETSKOV. Isothiazoles in the Design and Synthesis of Biologically Active Substances and Ligands for Metal Complexes[J]. Synthesis-Stuttgart, 2019, 113 1: 159-188. DOI:10.1055/s-0039-1690688.
[3] BERA A, PATRA P, AZAD A, et al. Neat synthesis of isothiazole compounds, and studies on their synthetic applications and photophysical properties?[J]. New Journal of Chemistry, 2022, 24: 11685-11694. DOI:10.1039/D2NJ01962K.
[4] ZHU-ZHU ZHANG. Synthesis of Isoselenazoles and Isothiazoles from Demethoxylative Cycloaddition of Alkynyl Oxime Ethers[J]. The Journal of Organic Chemistry, 2020, 86 1: 632-642. DOI:10.1021/acs.joc.0c02286.
Isothiazole Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Isothiazole manufacturers
- Product
- Isothiazole 288-16-4
- Price
- US $10.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 1000
- Release date
- 2024-03-26
- Product
- Isothiazole 288-16-4
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 500000kg
- Release date
- 2024-10-30
- Product
- Isothiazole 288-16-4
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 50000KG/month
- Release date
- 2023-11-23