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2-Azabicyclo[2.2.1]heptane-3-carboxylic acid, methylester (9CI) is a bicyclic azabicyclo compound characterized by a five-membered nitrogen-containing ring fused to a six-membered ring. This unique structural feature endows it with potential biological activity and makes it a valuable building block in organic synthesis and pharmaceutical research.

88260-07-5

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88260-07-5 Usage

Uses

Used in Pharmaceutical Research:
2-Azabicyclo[2.2.1]heptane-3-carboxylic acid, methylester (9CI) is used as a key intermediate in the development of medicinal drugs, particularly for the synthesis of antibiotics and pharmaceuticals targeting central nervous system disorders. Its unique structural properties contribute to the design and synthesis of novel drug candidates with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Azabicyclo[2.2.1]heptane-3-carboxylic acid, methylester (9CI) serves as a versatile intermediate for the synthesis of various functionalized organic molecules. Its presence in the molecular structure allows for the creation of diverse chemical entities with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 88260-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,6 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88260-07:
(7*8)+(6*8)+(5*2)+(4*6)+(3*0)+(2*0)+(1*7)=145
145 % 10 = 5
So 88260-07-5 is a valid CAS Registry Number.

88260-07-5SDS

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 methyl 3-azabicyclo[2.2.1]heptane-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-carbomethoxy-2-azabicyclo<2.2.1>heptane

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:88260-07-5 SDS

88260-07-5Downstream Products

88260-07-5Relevant academic research and scientific papers

Synthesis of potential thromboxane A2 antagonists based on the aza-bicycloheptane skeleton

Perrin, Veronique,Riveron, Veronique,Traversa, Christel,Balme, Genevieve,Gore, Jacques

, p. 3121 - 3145 (2007/10/03)

Thirteen compounds having a 2-aza or a 7-aza bicycloheptane framework substituted on carbon-3 by a prostanoic chain have been synthesized starting from easily obtained hetero-Diels Alder adducts. Due to their structure, a TxA2 antagonist

2-Azabicycloheptane-3-carboxylic Acid - A Bicyclic Proline

Gaitanopoulos, Dimitri E.,Weinstock, Joseph

, p. 957 - 959 (2007/10/02)

Diels-Alder reaction of cyclopentadiene and methyl N-carbobenzyloxy-2-iminoacetate generated in situ from methyl 2-chloro-N-carbobenzyloxyglycinate by triethylamine gave the N-carbobenzyloxy unsaturated bicyclic proline ester.This was converted in two ste

Total Synthesis of (+/-)-8-Aza-9a,9b-dicarbaprostaglandin H1

Blondet, Dominique,Morin, Christophe

, p. 1085 - 1090 (2007/10/02)

The total synthesis of a stable prostaglandin H1 analogue in which the bicyclic peroxide system is replaced by a 2-azabicycloheptane ring is described.Appropriate functionalization of the heterocycle and de-ethoxycarbonylation of an α-tr

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