Welcome to LookChem.com Sign In|Join Free

CAS

  • or

834-97-9

Post Buying Request

834-97-9 Suppliers

Recommended suppliersmore

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

834-97-9 Usage

Physical state

Colorless liquid the compound's appearance and phase (liquid) at room temperature.

Solubility

Insoluble in water the compound does not dissolve well in water, which may affect its reactivity and applications.

Boiling point

227-229°C the temperature range at which the compound changes from a liquid to a gas.

Uses

Synthesis of pharmaceuticals and agrochemicals the compound serves as a building block for creating other organic compounds used in drugs and pesticides.

Intermediate in dye production

The compound is used as an intermediate in the production of various dyes, contributing to its importance in the chemical industry.

Solvent in chemical reactions

1-chlorocyclohexanecarbonitrile can act as a solvent in various chemical reactions, aiding in the process and increasing efficiency.

Hazardous properties

Toxic and flammable the compound poses health and safety risks due to its toxic nature and ability to burn easily.

Handling precautions

Should be handled with care proper safety measures and precautions must be taken when working with 1-chlorocyclohexanecarbonitrile to minimize exposure and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 834-97-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 834-97:
(5*8)+(4*3)+(3*4)+(2*9)+(1*7)=89
89 % 10 = 9
So 834-97-9 is a valid CAS Registry Number.

834-97-9Downstream Products

834-97-9Relevant articles and documents

Acid-catalyzed Ethanolysis of Di-1-azulenyl Ketones

Saitoh, Masaki,Hashimoto, Keitaro,Nakazawa, Tomoo,Sugihara, Yoshikazu

, p. 3563 - 3566 (2007/10/02)

Substituted di-1-azulenyl ketones composed of 3,8-dimethyl-5-isopropyl-1-azulenyl and/or 4,6,8-trimethyl-1-azulenyl group were refluxed in ethanol in the presence of p-toluenesulfonic acid to give substituted azulenes and ethyl azulene-1-carboxylates derived from the cleavage of either of C-CO bonds of di-1-azulenyl ketones.The facility and the product distributions of the ethanolysis were affected markedly by the substitutents.

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

What can I do for you?
Get Best Price

Get Best Price for 834-97-9