92398-50-0

Basic information

• Product Name: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE
• Synonyms: Cycloheptanecarboxylic acid, 1-amino-, methyl ester, hydrochloride
• CAS NO: 92398-50-0
• Molecular Formula: C₉H₁₇NO₂*ClH
• Molecular Weight: 171.23678
• Mol File: 92398-50-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(92398-50-0)
• EPA Substance Registry System: METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE(92398-50-0)

Safety Data

• Hazardous Substances Data: 92398-50-0(Hazardous Substances Data)

Usage

General Description

Methyl 1-amino-1-cycloheptanecarboxylate is a chemical compound that belongs to the class of organic compounds known as amino acids and derivatives. It is a derivative of the amino acid ornithine and is commonly used in the synthesis of pharmaceuticals and in organic chemical reactions. METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE has a cycloheptane ring structure and contains both an amino group and a carboxylate group, making it a versatile building block for the preparation of various complex molecules. Its molecular structure and properties make it suitable for use in medicinal chemistry and chemical research, where it can be employed in the development of new drugs and materials. Overall, methyl 1-amino-1-cycloheptanecarboxylate is a valuable compound with diverse chemical applications.

Upstream product

• 67-56-1 methanol 
• 6949-77-5 1-aminocycloheptane-1-carboxylic acid 
• 707-16-4 1,3-diaza-spiro[4.6]undecane-2,4-dione 
• 502-42-1 cycloheptanone 

Downstream Products

• 92398-64-6 N-(benzyloxycarbonyl)-β-benzyl-L-aspartyl-α-aminocycloheptanecarboxylic acid methyl ester 
• 887243-88-1 methyl 1-{[(4-fluoro-2-nitrophenyl)carbonyl]amino}cycloheptanecarboxylate 
• 887243-93-8 methyl 1-({[4'-(methyloxy)-3-nitro-4-biphenylyl]carbonyl}amino)cycloheptanecarboxylate 
• 1298046-05-5 1-(3-acetoxy-4-methoxy-benzoylamino)-cycloheptanecarboxylic acid methyl ester 
• 1298046-34-0 1-[3-(2,2-difluoro-2-phenyl-ethoxy)-4-methoxy-benzoylamino]-cycloheptanecarboxylic acid methyl ester 
• 1298047-78-5 1-(3-hydroxy-4-methoxy-benzoylamino)-cycloheptanecarboxylic acid methyl ester 
• 1298046-06-6 1-{3-[2-(5-chloro-2-fluoro-phenyl)-ethoxy]-4-methoxy-benzoylamino}-cycloheptanecarboxylic acid methyl ester 
• 1298046-24-8 1-(4-acetyl-3-hydroxy-benzoylamino)-cycloheptanecarboxylic acid methyl ester 
• 1298046-26-0 1-(3-acetoxy-4-chloro-benzoylamino)-cycloheptanecarboxylic acid methyl ester 
• 1298046-04-4 1-{3-[2-(2-fluoro-5-methyl-phenyl)-ethoxy]-4-methoxy-benzoylamino}-cycloheptanecarboxylic acid methyl ester 
• 1298046-53-3 1-(3-{2-[3-(2-hydroxy-ethyl)-phenyl]-ethoxy}-4-methoxy-benzoylamino)-cycloheptanecarboxylic acid methyl ester 
• 1612148-87-4 methyl 1-({[1-(7-chloroquinolin-4-yl)-5-(2,6-dimethoxyphenyl)-1H-pyrazol-3-yl]carbonyl}amino)cycloheptanecarboxylate 
• 1190962-67-4 2'-((4-bromophenyl)amino)-spiro[cycloheptane-1,7'-pyrrolo[3,4-d]pyrimidin]-5'(6'H)-one 
• 1190962-03-8 2'-((4-(1-piperazinyl)phenyl)amino)spiro[cycloheptane-1,7'-pyrrolo[3,4-d]pyrimidin]-5'(6'H)-one 

Relevant articles and documents

Tropane alkaloid and synthesis method thereof

The invention relates to the technical field of chemical synthesis, and a tropane alkaloid and a synthesis method thereof are particularly disclosed. The structure formula (I) of the target product scopolamine alkaloid is described in the description, the

Ultrasound accelerated synthesis of proteinogenic and α,α- dialkylamino acid ester salts

A simple and efficient sonochemical esterification of proteinogenic as well as cyclic α,α-dialkyl amino acid methyl and ethyl ester hydrochloride salts employing thionyl chloride and alcohol has been reported. All the amino acid esters made have been obtained in good yield (94-98%) as pure compounds.

Peptide Sweeteners. 6. Structural Studies on the C-Terminal Amino Acid of L-Aspartyl Dipeptide Sweeteners

Stereochemical and structural aspects of the variations in the C-terminal residue of L-aspartyl-L-phenylalanine methyl ester have been investigated.Novel configurational analogues such as L-aspartyl-D-alanine benzyl ester and L-aspartyl-D-α-aminobutyric acid benzyl ester were found to be sweet.In addition, chiral and achiral α,α-dialkylglycine and α-aminocycloalkanecarboxylic acids were incorporated into the dipeptides.The L-aspartic acid based dipeptide derivatives of α-aminoisobutyric acid methyl ester, α-aminocyclopropanecarboxylic acid methyl ester, α-aminocyclobutanecarboxylic acid methyl ester, and α-aminocyclopentanecarboxylic acid methyl ester are sweet.Dipeptides with α-aminocyclohexanecarboxylic acid methyl ester and α-aminocycloheptanecarboxylic acid methyl ester are bitter, whereas the analogues with α-aminocyclooctanecarboxylic acid methyl ester, α,α-diethylglycine methyl ester, and α-aminoisobutyric acid benzyl ester are tasteless.Aspects on chirality and effective volume of the C-terminal residue are discussed and correlated with taste.