16441-25-1

Basic information

• Product Name: (2-PHENYL-1,3-THIAZOL-4-YL)ACETONITRILE
• Synonyms: 2-(2-Phenylthiazol-4-yl)acetonitrile
• CAS NO: 16441-25-1
• Molecular Formula: C₁₁H₈N₂S
• Molecular Weight: 200.26
• Mol File: 16441-25-1.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 386.9°Cat760mmHg
• Flash Point: 187.8°C
• Appearance: /
• Density: 1.223g/cm³
• Vapor Pressure: 3.42E-06mmHg at 25°C
• Refractive Index: 1.61
• CAS DataBase Reference: (2-PHENYL-1,3-THIAZOL-4-YL)ACETONITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: (2-PHENYL-1,3-THIAZOL-4-YL)ACETONITRILE(16441-25-1)
• EPA Substance Registry System: (2-PHENYL-1,3-THIAZOL-4-YL)ACETONITRILE(16441-25-1)

Safety Data

• Hazardous Substances Data: 16441-25-1(Hazardous Substances Data)

Usage

General Description

(2-phenyl-1,3-thiazol-4-yl)acetonitrile is a chemical compound with the molecular formula C11H8N2S. It is classified as a thiazole derivative, which is a type of heterocyclic compound containing a five-membered ring with sulfur and nitrogen atoms. (2-PHENYL-1,3-THIAZOL-4-YL)ACETONITRILE is commonly used in organic synthesis as a building block or intermediate in the production of various pharmaceuticals and agrochemicals. It may also exhibit biological activity and is used in the research and development of new drugs. Additionally, (2-phenyl-1,3-thiazol-4-yl)acetonitrile may have other industrial applications and uses in the field of organic chemistry.

InChI:InChI=1/C11H8N2S/c12-7-6-10-8-14-11(13-10)9-4-2-1-3-5-9/h1-5,8H,6H2

Upstream product

• 2227-79-4 benzenecarbothioamide 
• 4771-31-7 2-phenyl-4-chloromethylthiazole 
• 72011-24-6 1,4,7,10,13,20-Hexaoxa<13.1>(1,2)benzenophan 
• 773837-37-9 sodium cyanide 
• 143-33-9 sodium cyanide 

Downstream Products

• 16441-28-4 (2-phenyl-1,3-thiazol-4-yl)acetic acid 

Relevant articles and documents

Synthesis and Insecticidal Activity of Novel Thiazole Acrylonitrile Derivatives

A series of novel thiazole acrylonitrile derivatives was designed and synthesized utilizing NC-510 as a precursor. Their structures were characterized by NMR spectrometry, MS, and elemental analysis. The results of bioassay indicated that some of these ti

Thiazolyl acrylonitrile compound and use thereof

The invention discloses a thiazolyl acrylonitrile compound with novel structure or stereoisomers thereof. The compound has a general formula as shown in a general formula I. R is selected from C1-C6 alkyl, halogenated C1-C6 alkyl, C3-C8 cycloalkyl and C1-

2- [...] azoly acrylonitrile compound and use thereof

The invention discloses a 2-chloro thiazolyl acrylonitrile compound or a stereisomer thereof with a novel structure. The structure of the compound is shown as the general formula I in the specification, wherein R is one of alkyl of C1-C6, halogenated alkyl of C1-C6, cycloalkyl of C3-C8 and alkoxy of C1-C6; Q is selected from the group shown as the specification; R1 is one of H, halogen, methyl and trifluoromethyl; R2 is one of H and halogen. The compound in the general formula I has excellent insect and mite killing activity, and can be used for preventing and controlling insects and mites.