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METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE is a versatile organic compound belonging to the class of amino acids and derivatives. It is a derivative of the amino acid ornithine, characterized by a cycloheptane ring structure with both an amino group and a carboxylate group. This unique molecular structure endows it with diverse chemical applications, particularly in the synthesis of pharmaceuticals and organic chemical reactions. Its properties make it a valuable building block for the preparation of complex molecules, suitable for use in medicinal chemistry and chemical research for the development of new drugs and materials.

92398-50-0

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92398-50-0 Usage

Uses

Used in Pharmaceutical Synthesis:
METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex molecular structures. Its cycloheptane ring and functional groups contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Chemical Reactions:
In the field of organic chemistry, METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE serves as a versatile building block for the preparation of a wide range of complex molecules. Its unique structure allows for various chemical modifications, making it a valuable compound for advancing chemical research and the creation of novel materials.
Used in Medicinal Chemistry Research:
METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE is utilized as a fundamental component in medicinal chemistry research, where it aids in the exploration of new drug candidates and the enhancement of existing therapeutic agents. Its structural features facilitate the design and synthesis of molecules with improved pharmacological properties and therapeutic potential.
Overall, METHYL 1-AMINO-1-CYCLOHEPTANECARBOXYLATE is a multifaceted compound with significant applications across various industries, particularly in the development and synthesis of pharmaceuticals, organic chemical reactions, and medicinal chemistry research. Its unique molecular structure and properties make it an indispensable tool in the advancement of scientific knowledge and the creation of innovative solutions in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 92398-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,9 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92398-50:
(7*9)+(6*2)+(5*3)+(4*9)+(3*8)+(2*5)+(1*0)=160
160 % 10 = 0
So 92398-50-0 is a valid CAS Registry Number.

92398-50-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-aminocycloheptane-1-carboxylate,hydrochloride

1.2 Other means of identification

Product number -
Other names methyl 1-aminocycloheptanecarboxylate hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92398-50-0 SDS

92398-50-0Downstream Products

92398-50-0Relevant academic research and scientific papers

A class of nitrogen-containing heterocyclic butane framework of non-natural amino acid derivative and its synthesis method (by machine translation)

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Paragraph 0052-0054, (2019/03/26)

The invention belongs to the technical field of chemical synthesis, in particular discloses a containing azetidine skeleton of the synthesis method of the non-natural amino acid derivatives, its target product non-natural amino acid derivatives of the formula such as the specification of the Chinese (I), (II), (III), (IV) and (V) as shown in the, in the formula compound is a nitrogen-containing heterocyclic butane framework of non-naturalα-,β- Andγ- Amino acid derivatives, nitrogen atom are 2 - pyridine carboxylic acid protection; carboxyl methyl esterification; formula (I) in order to contain the azetidine framework of non-naturalα- Amino acid derivatives; (II) for the formula containing azetidine bridge ring skeleton of non-naturalα- Amino acid derivatives, wherein n=1 or 2; type (III) is a nitrogen-containing heterocyclic butane and ring skeleton of non-naturalα- Amino acid derivatives; formula (IV) is a nitrogen-containing heterocyclic butane bridge ring skeleton of non-naturalβ- Amino acid derivatives; type (V) is a nitrogen-containing heterocyclic butane and ring skeleton of non-naturalγ- Amino acid derivatives. The experiment of this invention result proves that: the compounds have potential hypolipidemic activity. (by machine translation)

Tropane alkaloid and synthesis method thereof

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Paragraph 0026; 0027; 0028, (2019/03/26)

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

Kantharaju,Babu, Vommina V. Suresh

, p. 1942 - 1944 (2007/10/03)

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.

Hydrogen-bonded tapes based on symmetrically substituted diketopiperazines: A robust structural motif for the engineering of molecular solids

Palacin, Serge,Chin, Donovan N.,Simanek, Eric E.,MacDonald, John C.,Whitesides, George M.,McBride, Mary T.,Palmore, G. Tayhas R.

, p. 11807 - 11816 (2007/10/03)

A series of eight symmetrically substituted diketopiperazines (DKPs) derived from 1-amino-1-carboxycycloalkanes (n = 3-7; 3,3,5,5-tetramethylcyclohexane; 4,4-dimethylcyclohexane; 2-indan) were synthesized and their crystal structures determined. In the solid state, all eight compounds form two pairs of hydrogen bonds with two adjacent molecules to form a one-dimensional structure that we refer to as 'tapes'. These molecules represent a range of volumes and shapes that contain a common molecular fragment (DKP ring). We examined this series of compounds with three objectives in mind: (i) to establish the ability of the hydrogen-bonded 'tape' motif to persist through these differences in volume and shape; (ii) to provide a series of structurally related compounds to use to test computational methods of predicting crystal structure from molecular structure; (iii) to search for qualitative correlations between molecular structure and crystal packing. All compounds form tapes and with one exception, all tapes pack with their long axes parallel. When viewed down their long axis, two types of tapes emerge: planar and nonplanar. The type of tape that forms reflects the conformation adapted by the DKP ring-planar or boat. Planar tapes form when the angle (α) between the two planes defined by the cis-amides in the DKP ring is 180°; nonplanar tapes form when α 180°. Five of the eight compounds studied form planar tapes, the remaining three compounds form nonplanar tapes. Despite the variability in volume and shape represented by this series of molecules, the persistence of the tape motif in their crystalline solids suggests that the hydrogen-bonding interactions between parallel alignment of tapes that pack in a manner that permits the interdigitation of substituents on adjacent tapes.

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

Tsang, Joseph W.,Schmied, Bernhard,Nyfeler, Rolf,Goodman, Murray

, p. 1663 - 1668 (2007/10/02)

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.

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