34960-41-3

Basic information

• Product Name: Cyclohexene, 4-(bromomethyl)-
• Synonyms: 3-cyclohexenylmethyl bromide;1-bromomethyl-3-cyclohexene;3-cyclohexenylbromomethane;1-bromomethylcyclohex-3-ene;bromomethylcyclohex-3-ene;4-bromomethylcyclohexene
• CAS NO: 34960-41-3
• Molecular Formula: C7H11Br
• Molecular Weight: 175.068
• Mol File: 34960-41-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 37 °C(Press: 2 Torr)
• Density: 1.331 g/cm3(Temp: 25 °C)
• CAS DataBase Reference: Cyclohexene, 4-(bromomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexene, 4-(bromomethyl)-(34960-41-3)
• EPA Substance Registry System: Cyclohexene, 4-(bromomethyl)-(34960-41-3)

Safety Data

• Hazardous Substances Data: 34960-41-3(Hazardous Substances Data)

Upstream product

• 4771-80-6 1,2,5,6-tetrahydrobenzoic acid 
• 100-50-5 3-Cyclohexene-1-carboxaldehyde 
• 108541-48-6 [(cyclohex-3-en-1-yl)methyl]methanesulfonate 
• 92864-78-3 cyclohex-3-en-1-ylmethyl 4-methylbenzenesulfonate 
• 72581-32-9 cyclohex-3-enylmethanol 

Downstream Products

• 24480-99-7 cyclohex-3-enyl acetaldehyde 
• 18240-10-3 (+/-)-2-(3-cyclohexenyl)ethanol 
• 125364-83-2 2-(cyclohexen-4-yl)methyl-1,3-oxathiolan-5-one 
• 10468-32-3 2-(cyclohex-3-en-1-yl)acetic acid 
• 84173-92-2 C₁₀H₁₆O₂ 
• 61880-14-6 N-Nitroso-N-methylcyclohex-3-enylmethylamin 
• 141814-72-4 4-Amino-5-chloro-N-(4-cyclohex-3-enylmethyl-morpholin-2-ylmethyl)-2-methoxy-benzamide 
• 141815-16-9 C-(4-Cyclohex-3-enylmethyl-morpholin-2-yl)-methylamine 
• 13407-18-6 4-Methylen-1-cyclohexen 
• 15908-04-0 N-Methyl-(3-cyclohexenylmethyl)amine 
• 108238-87-5 2-acetylamino-2-cyano-3-cyclohex-3-enyl-propionic acid ethyl ester 
• 1266663-16-4 C₁₄H₁₆O₂ 
• 1266663-18-6 C₁₈H₂₄O₂ 
• 1266663-17-5 C₁₈H₂₆O₃ 

Relevant articles and documents

Compound with dual inhibitory activity TDO, IDOO1 and application of compound for treating neurodegenerative disease (by machine translation)

The present invention provides a compound of formula I, or a pharmaceutically acceptable salt thereof, or a solvate thereof, which can selectively inhibit TDO, IDOO1, which has a significant inhibitory effect on TDO and/or IDOO1. In addition, the prepared compound has a remarkable anti-tumor effect, has a certain treatment effect on's disease and's disease, and has a good application prospect in the field of medicine preparation. (by machine translation)

cis-dihydroxylation of unsaturated potassium alkyl- and aryltrifluoroborates

(Chemical Equation Presented) The cis-dihydroxylation of olefin-containing potassium alkyl- and aryltrifluoroborates proceeds readily in moderate to excellent yields. The resulting diols are efficient coupling partners in Suzuki-Miyaura-type reactions wit

REACTION OF (TRIMETHYLSTANNYL)COPPER(I) REAGENTS WITH α,β-ACETYLENIC ESTERS. STEREOCONTROLLED SYNTHESIS OF ALKYL (E)- AND (Z)-3-TRIMETHYLSTANNYL-2-ALKENOATES

The reactions of α,β-acetylenic esters 1 with the (trimethylstannyl)copper(I) reagents 4-7 provide good to excellent yields of the corresponding β-trimethylstannyl α,β-unsaturated esters 10 and (or) 11.In nearly all cases studied, except for the reactions