1001847-95-5

Basic information

• Product Name: 2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate
• Synonyms: 2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate
• CAS NO: 1001847-95-5
• Molecular Weight: 215.319
• Mol File: 1001847-95-5.mol

Chemical Properties

• CAS DataBase Reference: 2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate(1001847-95-5)
• EPA Substance Registry System: 2-(3,3-dimethylbut-1-ynyl)phenyl isothiocyanate(1001847-95-5)

Safety Data

• Hazardous Substances Data: 1001847-95-5(Hazardous Substances Data)

Upstream product

• 917-92-0 3,3-Dimethylbut-1-yne 
• 615-43-0 2-iodophenylamine 
• 116491-51-1 2-(3,3-dimethyl-1-butynyl)aniline 
• 75-15-0 carbon disulfide 
• 207278-63-5 2-(3,3-dimethyl-1-butynyl)-N-(triphenylphosphonylidene)benzeneamine 

Downstream Products

• 1001848-06-1 4-(4-bromophenyl)-2(1H)-quinolinethione 
• 1001848-01-6 4-(5-methoxy-2-methylphenyl)-2(1H)-quinolinethione 
• 1001848-00-5 4-(2-methoxy-5-methylphenyl)-2(1H)-quinolinethione 
• 1001848-02-7 4-(5-bromo-2-methoxyphenyl)-2(1H)-quinolinethione 
• 1001847-98-8 4-(4-phenoxyphenyl)-2(1H)-quinolinethione 
• 1001848-07-2 4-phenylthio-2(1H)-quinolinethione 
• 1001848-09-4 4-(4-methylphenyl)thio-2(1H)-quinolinethione 
• 1001848-08-3 4-(4-thiophenoxyphenyl)-2(1H)-quinolinethione 
• 1001847-97-7 4-(2-methoxyphenyl)-2(1H)-quinolinethione 
• 1001847-96-6 4-(4-methoxyphenyl)-2(1H)-quinolinethione 
• 1001848-05-0 4-(2-methylphenyl)-2(1H)-quinolinethione 
• 1001848-04-9 4-(4-methylphenyl)-2(1H)-quinolinethione 
• 1001847-99-9 4-(2,5-dimethoxyphenyl)-2(1H)-quinolinethione 
• 21112-37-8 1,4-dimethoxy-2-tert-butylbenzene 

Relevant articles and documents

Nickel Catalysis Enables Hetero [2+2+1] Cycloaddition between Yne-Isothiocyanates and Isonitriles with Low Catalyst Loading

Nickel(II) can be used to catalyze the hetero [2+2+1] cycloaddition of 2-alkynylaryl isothiocyanates and isonitriles in 2-methyltetrahydrofuran (2-MeTHF) to give a wide array of thieno[2,3-b]indoles in excellent yields. The reaction is featured by employi

Triflic acid-promoted cycloisomerization of 2-alkynylphenyl isothiocyanates and isocyanates: A novel synthetic method for a variety of indole derivatives

A new approach towards the synthesis of indole derivatives via triflic acid-promoted cycloisomerization with rearrangement of 2-(alkyn-1-yl)phenyl isothiocyanates and 2-(alkyn-1-yl)phenyl isocyanates has been achieved. By this methodology, structurally di

TfOH-promoted transformation from 2-alkynylphenyl isothiocyanates to quinoline-2-thiones or indoles

A variety of 4-arylquinoline-2-thiones and 3-arylthieno[2,3-b]indoles were synthesized in high yields via TfOH-promoted tandem Friedel-Crafts alkenylation-cyclization reactions of 2-alkynylphenyl isothiocyanates.

Thiocarbonyl induced heterocumulenic Pauson-Khand type reaction: Expedient synthetic method for thieno[2,3-b]indol-2-ones

The first examples of C=S induced Pauson-Khand type reactions are described; 2-alkynylphenyl isothiocyanates were converted to 3-substituted-2H-thieno[2,3-b]indol-2-ones in the presence of a stoichiometric amount of Mo(CO)6 or Co2(CO