216574-58-2

Usage

Uses

Used in Pharmaceutical Industry:
3-CHLORO-4,4-DIMETHYLPENT-2-ENENITRILE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-CHLORO-4,4-DIMETHYLPENT-2-ENENITRILE is utilized as a precursor in the production of agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Dye and Pigment Production:
3-CHLORO-4,4-DIMETHYLPENT-2-ENENITRILE is employed as a building block in the creation of dyes and pigments, playing a significant role in the coloration of various materials and products.
Used in Organic Compound Synthesis:
This chemical is also used as a precursor in the synthesis of other organic compounds, broadening its applications across different industries that rely on organic chemistry for product development.
Safety Considerations:
Given its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system, 3-CHLORO-4,4-DIMETHYLPENT-2-ENENITRILE requires careful handling and the implementation of proper safety measures during its use in various applications.

InChI:InChI=1/C7H10ClN/c1-7(2,3)6(8)4-5-9/h4H,1-3H3/b6-4-

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 68-12-2 N,N-dimethyl-formamide 
• 4302-24-3 3-chloro-4,4-dimethylpent-2-enal 

Downstream Products

• 175137-03-8 methyl 3-amino-5-tert-butylthiophene-2-carboxylate 
• 216574-57-1 methyl 3-amino-5-tert-butylfuran-2-carboxylate 
• 1380808-99-0 [6-(tert-butyl)selenopheno[2,3-e]pyrimidin-4-yl](3-chloro-4-fluorophenyl)amine 
• 175137-04-9 3-amino-5-(tert-butyl)thiophene-2-carboxamide 
• 677277-39-3 5-tert-butyl-3-aminothiophene-2-carbonitrile 

Relevant academic research and scientific papers

SUBSTITUTED 4-(SELENOPHEN-2(OR-3)-YLAMINO)PYRIMIDINE COMPOUNDS AND METHODS OF USE THEREOF

Selenophene compounds of formula (I) are described herein. In the compounds of Formula (I), ring A is a 6-membered aromatic fused ring, optionally containing one, two or three nitrogen atoms; a 5-membered heteroaromatic fused ring; or a mono- or bicyclic

ANTI-CANCER DRUGS, AND USES RELATING FOR MALIGNANT MELANOMA AND OTHER CANCERS

Selenopheno triazene analogs, their compositions, tautomeric forms, stereoisomers, polymorphs, hydrates, solvates, and pharmaceutically acceptable salts and mixtures thereof are useful for the treatment of metastatic malignant melanoma and other cancers. The selenopheno triazene analogs have the general formulae (I) or (II): wherein the substituents R1, R2, R3, R6, and R7 are as described in the specification. Other cancers include which may be treated with these compounds include, but are not limited to, malignant melanoma, leukemia, lymphomas (Hodgkins and non-Hodgkins), sarcomas (Ewing's sarcoma), brain tumors, central nervous system (CNS) metastases, gliomas, carcinomas such as breast cancer, prostate cancer, lung cancer (small cell and non-small cell), colon cancer, pancreatic cancer, Head and Neck cancers and oropharyngeal squamous cell carcinoma.

Synthesis of a novel series of thieno[3,2-d]pyrimidin-4-(3H)-ones

2-Aminothieno[3,2-d]pyrimidin-4-ones were synthesized in one step by condensation of 3-amino(benzo)thiophene car-boxylate with chloroformamidine hydrochloride. Georg Thieme Verlag Stuttgart.

Synthesis of selenophene analogues of the tacrine series: Comparison of classical route and microwave irradiation

New 3-amino-2-selenophenecarbonitriles condensed with cyclanones to afford, in one step, analogues of Tacrine. A comparison between classical heating and microwave irradiation for the Friedlaender condensation is presented. Georg Thieme Verlag Stuttgart.

Synthesis of new thieno[b]azepinediones from α-methylene ketones

New substituted 6,7-dihydro-4H-thieno[3,2-b]azepine-5,8-diones were synthesized in seven steps, starting from substituted α-methylene ketones, via 3-aminothiophene-2-carboxylic acid alkyl esters.