Welcome to LookChem.com Sign In|Join Free
  • or
1-Chloro-4-methylbicyclo[2.2.2]octane is a chemical compound with the molecular formula C9H15Cl. It is a halogenated derivative of a bicyclic hydrocarbon, specifically a bicyclo[2.2.2]octane, which features a unique cage-like structure with two carbon-carbon double bonds. The compound is characterized by the presence of a chlorine atom attached to one of the carbon atoms and a methyl group on another, which can influence its reactivity and physical properties. It is an organic compound that can be used in various chemical syntheses and as an intermediate in the production of pharmaceuticals and other organic compounds. Due to its specific structure and functional groups, 1-chloro-4-methylbicyclo[2.2.2]octane may exhibit unique chemical behaviors and reactivity patterns, making it a potentially valuable compound in organic chemistry research and industrial applications.

7697-06-5

Post Buying Request

7697-06-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7697-06-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7697-06-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7697-06:
(6*7)+(5*6)+(4*9)+(3*7)+(2*0)+(1*6)=135
135 % 10 = 5
So 7697-06-5 is a valid CAS Registry Number.

7697-06-5Downstream Products

7697-06-5Relevant academic research and scientific papers

Transmission of Polar Substituent Effects Through the Bicyclooctane Ring System as Monitored by NMR Shifts: a 13C NMR Study of 4-Substituted-1-methylbicyclooctanes

Adcock, William,Abeywickrema, Anil N.,Iyer, V. Sankar,Kok, Gaik B.

, p. 213 - 220 (2007/10/02)

Carbon-13 substituent chemical shifts (SCS) are reported for the methyl group of a series of 4-substituted 1-methylbicyclooctanes covering a wide range of electronic substituent effects.Unlike the 13C SCS of the α-carbon centre in various unsaturat

SYNTHESIS OF BRIDGEHEAD CHLORO-, BROMO- AND IODOBICYCLOOCTANES

Kopecky, Jan,Smejkal, Jaroslav

, p. 2965 - 2970 (2007/10/02)

The paper describes transformations of hydroxy-, acetoxy- or methoxy-bridgehead bicyclooctanes into bridgehead chloro, bromo or iodo derivatives by action of inorganic halides in the medium of orthophosphoric or polyphosphoric acids.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7697-06-5