3419-73-6

Basic information

• Product Name: tert-butyl Cyclohexene benzene
• Synonyms: tert-butyl Cyclohexene benzene;1-Phenyl-4-tert-butyl-1-cyclohexene
• CAS NO: 3419-73-6
• Molecular Formula: C₁₆H₂₂
• Molecular Weight: 214.34588
• Mol File: 3419-73-6.mol
• Article Data: 20

Chemical Properties

• Boiling Point: 106-107℃ (0.4 Torr)
• Flash Point: 130.9±7.6℃
• Appearance: /
• Density: 0.939±0.06 g/cm3 (20 ºC 760 Torr)
• Refractive Index: 1.5437 (589.3 nm 20℃)
• CAS DataBase Reference: tert-butyl Cyclohexene benzene(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl Cyclohexene benzene(3419-73-6)
• EPA Substance Registry System: tert-butyl Cyclohexene benzene(3419-73-6)

Safety Data

• Hazardous Substances Data: 3419-73-6(Hazardous Substances Data)

Upstream product

• 57466-12-3 4-tert-butyl-1-methoxycyclohexene 
• 21024-55-5 trans-4-tert-butyl-1-phenylcyclohexanol 
• 17807-26-0 cis-4-tert-butyl-1-phenylcyclohexanol 
• 98-80-6 phenylboronic acid 
• 100-58-3 phenylmagnesium bromide 
• 98-53-3 4-tercbutyl-cyclohexanone 
• 100-59-4 phenylmagnesium chloride 
• 611235-47-3 toluene-4-sulfonic acid 4-tert-butylcyclohex-1-en-1-yl ester 
• 6832-09-3 1-chloro-4-tert-butylcyclohexene 
• 119061-98-2 1-(tributylstannyl)-4-tert-butylcyclohexene 
• 63031-67-4 4-(1,1-dimethylethyl)cyclohexen-1-yltrimethylsilane 
• 536-80-1 iodosylbenzene 
• 77412-96-5 1-trifluoromethanesulfonyloxy-4-t-butylcyclohexene 
• 591-51-5 phenyllithium 

Downstream Products

• 407593-31-1 (1R,2R,4S)-1-phenyl-4-tert-butylcyclohexan-1,2-diol 
• 4127-41-7 1-phenyl-4-tert-butylcyclohexan-1,2-diol 
• 407593-29-7 1-Phenyl-cis-4-tert.-butyl-cyclohexan-cis-1,2-diol 
• 4341-22-4 1-phenyl-cis-4-t-butyl-1,2-epoxycyclohexane 
• 87830-02-2 r-1-phenyl-1-fluoro-c-2-bromo-t-4-tert-butylcyclohexane 

Relevant articles and documents

A NEW METHOD OF OLEFIN SYNTHESIS. COUPLING OF LITHIUM DIALKYLCUPRATES WITH ENOL TRIFLATES

Enol trifluoromethanesulfonates react with lithium dialkylcuprates to give the coupling products in high yields.The reaction is stereoselective and is successful with a wide variety of organocuprates , including methyl, butyl, phenyl, vinyl, and cycloprop

Supramolecular Assembly of Complementary Cyanine Salt J-Aggregates

An understanding of structure-property relationships in cyanine dyes is critical for their design and application. Anionic and cationic cyanines can be organized into complementary cyanine salts, offering potential building blocks to modulate their intra/

Iodine induced transformations of alcohols under solvent-free conditions

Iodine has been shown to be an efficient catalyst for transformations of alcohols under solvent-free conditions. In the presence of 5% of iodine, tertiary alcohols underwent dehydration forming the corresponding alkenes, while in the case of 2-phenylpropane-2-ol cyclodimerisation to 1,1,3-trimethyl-3-phenylindane took place. Secondary and primary benzyl alcohols under the same conditions gave the corresponding ethers.