19509-49-0

Basic information

• Product Name: 3-Chloromethyl-1-cyclohexene
• Synonyms: 3-Chloromethyl-1-cyclohexene
• CAS NO: 19509-49-0
• Molecular Formula: C₇H₁₁Cl
• Molecular Weight: 0
• Mol File: 19509-49-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Chloromethyl-1-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloromethyl-1-cyclohexene(19509-49-0)
• EPA Substance Registry System: 3-Chloromethyl-1-cyclohexene(19509-49-0)

Safety Data

• Hazardous Substances Data: 19509-49-0(Hazardous Substances Data)

Upstream product

• 286-08-8 bicyclo[4.1.0]heptane 
• 103668-33-3 3-hydroxymethylcyclohexene 
• 63262-74-8 cyclohex-2-en-1-ylmethyl 4-methylbenzenesulfonate 
• 7432-49-7 endo-2-norcaranol 
• 2441-97-6 3-chloro-cyclohexene 
• 157-22-2 diazirine 
• 7639-16-9 di(trans-2-chlorocyclohexylmethyl)formal 
• 7641-25-0 Formaldehyd-bis- 
• 7639-12-5 trans-1-hydroxymethyl-2-chlorocyclohexane 

Downstream Products

• 16452-34-9 2-(cyclohex-2-enyl)ethanol 
• 591-48-0 3-methyl-1-cyclohexene 
• 96333-89-0 2-cyclohex-2-en-1-yl-1-phenylethanol 
• 96333-87-8 1-(2-cyclohexenyl)-2-propanol 
• 96333-88-9 1-Cyclohex-2-enyl-pentan-2-ol 
• 19509-51-4 3-(β-chloroethyl)cyclohexene 
• 96333-90-3 3-(2-chloropropyl)cyclohexene 
• 96333-91-4 3-(2-Chloro-pentyl)-cyclohexene 
• 19642-38-7 2-(cyclohex-2-en-1-yl)ethanethiol 
• 120698-10-4 1-Cyclohex-2-enyl-propane-2-thiol 
• 120698-11-5 1-Cyclohex-2-enyl-pentane-2-thiol 
• 120698-12-6 2-Cyclohex-2-enyl-1-phenyl-ethanethiol 
• 96333-92-5 (1-Chloro-2-cyclohex-2-enyl-ethyl)-benzene 
• 96333-94-7 (2S,3aR,7aR)-2-Phenyl-octahydro-benzo[b]thiophene 

Relevant articles and documents

C-HALOGEN BOND FORMATION

Methods of halogenating a carbon containing compound having an sp3 C-H bond are provided. Methods of fluorinating a carbon containing compound comprising halogenation with Cl or Br followed by nucleophilic substitution with F are provided. Methods of direct oxidative C-H fluorination of a carbon containing compound having an sp3 C-H bond are provided. The halogenated products of the methods are provided.

Stereodirecting effects in the characterization of ylide intermediates in reactions of singlet methylene with an allylic ether and an allylic chloride

The stereodirecting effects of substrate substituents were examined in addition of 1:CH2 to the double bonds of 3-methoxycyclohexene (3a), 3-chlorocyclohexene (3b), and 3-methylcyclohexene (3c) in pentane solution at temperatures fro

PREPARATIVE SYNTHESIS OF PRIMARY AND SECONDARY ALKYL CHLORIDES FROM ALCOHOLS

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