765262-90-6

Basic information

• Product Name: Cyclohexanecarboxylic acid, 1-amino-4-methoxy-, methyl ester, trans- (9CI)
• Synonyms: Cyclohexanecarboxylic acid, 1-amino-4-methoxy-, methyl ester, trans- (9CI)
• CAS NO: 765262-90-6
• Molecular Formula: C9H17NO3
• Molecular Weight: 187.23618
• Product Categories: METHOXY;AMINOACID
• Mol File: 765262-90-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 243.0±40.0°C at 760 mmHg
• Flash Point: 79.9±23.7°C
• Appearance: /
• Density: 1.1±0.1g/cm3
• CAS DataBase Reference: Cyclohexanecarboxylic acid, 1-amino-4-methoxy-, methyl ester, trans- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxylic acid, 1-amino-4-methoxy-, methyl ester, trans- (9CI)(765262-90-6)
• EPA Substance Registry System: Cyclohexanecarboxylic acid, 1-amino-4-methoxy-, methyl ester, trans- (9CI)(765262-90-6)

Safety Data

• Hazardous Substances Data: 765262-90-6(Hazardous Substances Data)

Upstream product

• 191110-78-8 syn/anti-1-[N-(t-butoxycarbonyl)amino]-4-hydroxycyclohexane-1-carboxylic acid methyl ester 
• 191111-27-0 methyl 1-((tert-butoxycarbonyl)amino)-4-oxocyclohexanecarboxylate 
• 104-94-9 4-methoxy-aniline 
• 124-38-9 carbon dioxide 
• 387825-55-0 cis-1-amino-4-methoxycyclohexane-1-carboxylic acid 
• 4342-46-5 1-amino-4-methoxycyclohexane 
• 387825-48-1 cis-8-methoxy-1,3-diazaspiro[4,5]-decane-2,4-dione 
• 67-56-1 methanol 
• 150-76-5 4-methoxy-phenol 
• 13482-23-0 4-methoxycyclohexanone 
• 387825-48-1 cis-8-methoxy-1,3-diazaspiro[4.5]decane-2,4-dione 
• 387825-55-0 cis-1-amino-4-methoxycyclohexane-1-carboxylic acid 

Relevant articles and documents

A High-Yield and Cost-Effective Synthesis of Spirotetramat

Abstract: cis-8-Methoxy-1,3-diazaspiro[4.5]decane-2,4-dione, the key intermediate in the synthesis of spirotetramat, was synthesized by catalytic hydrogenation, oxidation, and Bucherer–Bergs reaction with 4-methoxycyclohexan-1-one as raw material. Spirotetramat was obtained in an overall yield of 20.4% by a multi-step reaction sequence including hydrolysis, esterification, acylation, intramolecular condensation, and O-acylation. The advantages of the proposed method are mild conditions, simple operation, and good to excellent yields in each step.

Preparation method and application of novel aminoazaheterocycles compound

The invention discloses a preparation method and application of a novel aminoazaheterocycles compound, and belongs to the technical field of applied chemistry. The technical scheme disclosed by the invention is characterized in that the novel aminoazaheterocycles compound has a following structure: a formula shown in the description. The invention further discloses the preparation method of the novel aminoazaheterocycles compound. The novel aminoazaheterocycles compound is synthesized through a new method; a reaction process is simple to operate and feasible, and raw materials are cheap and easy to obtain; the reaction efficiency is relatively high, and the repeatability is relatively good; the insecticidal activity effect is obvious.

Novel preparation method of spirotetramat

The invention discloses a novel preparation method of spirotetramat and belongs to the technical field of pesticide syntyesis. The key point of the technical scheme is as follows: the method is characterized by carrying out cyclization reaction via 1-amin