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15210-60-3

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15210-60-3 Usage

Description

Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride is a complex organic compound with a unique tricyclic structure and three methyl groups at the 3rd, 5th, and 7th positions. It is a derivative of the parent compound, tricyclo[3.3.1.13,7]decan-1-amine, and the hydrochloride salt form enhances its solubility and stability. Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride has potential applications in various fields due to its chemical properties and structural characteristics.

Uses

Used in Pharmaceutical Industry:
Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride is used as an active pharmaceutical ingredient (API) for the development of drugs targeting neurological disorders. Its unique structure allows it to interact with specific receptors in the nervous system, potentially providing therapeutic benefits for conditions such as Parkinson's disease and spasticity.
Used in Chemical Research:
In the field of chemical research, Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride serves as a valuable compound for studying the effects of structural modifications on the properties and reactivity of organic molecules. It can be used as a starting material for the synthesis of more complex molecules with potential applications in various industries.
Used in Material Science:
The unique structural features of Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride make it a candidate for the development of novel materials with specific properties. It can be used as a building block in the synthesis of advanced materials for applications in areas such as electronics, optics, and energy storage.
Used in Impurity Analysis:
As an impurity of Memantine (HCl salt, M218000), Tricyclo[3.3.1.13,7]decan-1-amine, 3,5,7-trimethyl-, hydrochloride is used in the quality control and analysis of Memantine, an antiparkinsonian and antispasmodic drug. Ensuring the purity and safety of pharmaceutical products is crucial, and this compound plays a role in monitoring and controlling the presence of impurities during the manufacturing process.

Check Digit Verification of cas no

The CAS Registry Mumber 15210-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,1 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15210-60:
(7*1)+(6*5)+(5*2)+(4*1)+(3*0)+(2*6)+(1*0)=63
63 % 10 = 3
So 15210-60-3 is a valid CAS Registry Number.
InChI:InChI=1S/C13H23N.ClH/c1-10-4-11(2)6-12(3,5-10)9-13(14,7-10)8-11;/h4-9,14H2,1-3H3;1H

15210-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,7-trimethyladamantan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 3,5,7-Trimethyladamantan-1-amine 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:15210-60-3 SDS

15210-60-3Downstream Products

15210-60-3Relevant articles and documents

One-Pot Amination of Cage Hydrocarbons

Leonova,Skomorokhov,Moiseev,Klimochkin

, p. 1703 - 1709 (2016/02/03)

A one-pot procedure has been proposed for the synthesis of amines directly from cage hydrocarbons. A number of cage amines have been synthesized by treatment of adamantane, its homologs, and structurally related cage hydrocarbons with nitric acid in acetic acid and subsequent addition of urea and heating.

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