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4-AMINOBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID METHYL ESTER is a synthetic chemical compound with the molecular formula C10H17NO2. It is a methyl ester derivative of the amino acid 4-aminobicyclo[2.2.2]octane-1-carboxylic acid, characterized by its unique bicyclic structure. 4-AMINOBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID METHYL ESTER is not commonly found in nature but is valued in the pharmaceutical industry for its potential applications in drug development and delivery.

135908-33-7

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135908-33-7 Usage

Uses

Used in Pharmaceutical Industry:
4-AMINOBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID METHYL ESTER is used as a building block for the synthesis of various drugs and biologically active compounds. Its unique structure allows for the creation of diverse molecular structures, making it a versatile intermediate in medicinal chemistry.
Used in Drug Delivery Systems:
Due to its potential interactions with biological systems, 4-AMINOBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID METHYL ESTER is studied for its use as a drug delivery system. This application aims to enhance the efficacy and targeted delivery of pharmaceuticals, potentially improving treatment outcomes for various conditions.
Used in Organic Synthesis:
4-AMINOBICYCLO[2.2.2]OCTANE-1-CARBOXYLIC ACID METHYL ESTER also serves as a valuable intermediate in organic synthesis, where it can be used to produce a wide range of chemical compounds for various applications, further expanding its utility in the chemical and pharmaceutical sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 135908-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,0 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135908-33:
(8*1)+(7*3)+(6*5)+(5*9)+(4*0)+(3*8)+(2*3)+(1*3)=137
137 % 10 = 7
So 135908-33-7 is a valid CAS Registry Number.

135908-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-aminobicyclo[2.2.2]octane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Aminobicyclo[2.2.2]octane-1-carboxylic acid methyl ester

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:135908-33-7 SDS

135908-33-7Relevant academic research and scientific papers

2,3-DIHYDRO-1H-PYRROLIZINE-7-FORMAMIDE DERIVATIVE AND APPLICATION THEREOF

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, (2021/04/16)

The present application relates to a 2,3-dihydro-1H-pyrrolizine-7-formamide derivative as a nucleoprotein inhibitor and a use in preparation of a drug for treating HBV related diseases. The present application specifically relates to a compound represented by formula (II), and isomers or pharmaceutically acceptable salts thereof.

NOVEL AMIDE AND AMIDINE DERIVATIVES AND USES THEREOF

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Page/Page column 33, (2010/11/03)

The present invention relates to inhibitors of 11-β-hydroxysteroid dehydrogenase type 1 enzyme and their use in treatment of non-insulin dependent type 2 diabetes, insulin resistance, obesity, lipid disorders, metabolic syndrome, central nervous system disorders, and diseases and conditions that are related to excessive glucocorticoids.

GUT MICROSOMAL TRIGLYCERIDE TRANSPORT PROTEIN INHIBITORS

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Page/Page column 123, (2008/12/08)

Compounds represented by formula (I): are inhibitors of gut microsomal triglyceride transfer protein. Such compounds are useful in treating diseases or conditions such as diabetes and obesity, along with patients are risk for developing such diseases or conditions.

Synthesis and structural activity relationship of 11β-HSD1 inhibitors with novel adamantane replacements

Yeh, Vince S.C.,Kurukulasuriya, Ravi,Madar, David,Patel, Jyoti R.,Fung, Steven,Monzon, Katina,Chiou, William,Wang, Jiahong,Jacobson, Peer,Sham, Hing L.,Link

, p. 5408 - 5413 (2007/10/03)

A series of structurally novel and metabolically stable bridged bicyclic carbocycle and heterocycle adamantane replacements have been synthesized and biologically evaluated. Several of these compounds exhibit excellent human and mouse 11β-HSD1 potency and

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