64374-26-1

Basic information

• Product Name: Acetamide, N-[1-[4-(acetylamino)-4-methylcyclohexyl]-1-methylethyl]-
• CAS NO: 64374-26-1
• Molecular Formula: C14H26N2O2
• Molecular Weight: 254.373
• Mol File: 64374-26-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[1-[4-(acetylamino)-4-methylcyclohexyl]-1-methylethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[1-[4-(acetylamino)-4-methylcyclohexyl]-1-methylethyl]-(64374-26-1)
• EPA Substance Registry System: Acetamide, N-[1-[4-(acetylamino)-4-methylcyclohexyl]-1-methylethyl]-(64374-26-1)

Safety Data

• Hazardous Substances Data: 64374-26-1(Hazardous Substances Data)

Upstream product

• 80-56-8 Pinene 
• 75-05-8 acetonitrile 
• 177698-19-0 Beta-pinene 
• 138-86-3 limonene. 
• 99-85-4 crithmene 
• 64374-25-0 1,8-Diazido-p-menthan 
• 64374-19-2 8-Azido-1-hydroxy-trans-p-menthan 
• 565-48-0 cis-1,8-terpine 
• 80-52-4 1,8-diamino-p-menthane 
• 108-24-7 acetic anhydride 

Relevant articles and documents

Method for preparing 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine from unsaturated turpentine monoterpene

The invention discloses a method for preparing 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine from unsaturated turpentine monoterpene. The unsaturated turpentine monoterpene is used as a raw material and takes a reaction with organic nitrile under the catalysis of strong protonic acid; after full reaction, reaction liquid is neutralized into a neutral state; a non-water-soluble organic solvent is added for extraction; an organic layer is collected and is subjected to still standing; 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine crystals are separated out. 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine solid is hydrolyzed in a polyatomic alcohol solution of inorganic strong base to obtain 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine crude products; negative pressure distillation is performed to obtain 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine pure products. The yield of the 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine product obtained by the method is high; the purity is high. Compared with the existing preparation method, the method has the advantages that the unsaturated turpentine monoterpene which has low cost and is easy to obtain is used as the raw material; the process route is simple; the production cost of the 4-amino-alpha, alpha,4-trimethyl-cyclohexanemethanamine can be effectively reduced; in addition, the method also has the advantages of low toxicity, simple operation process and the like.