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697-25-6

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697-25-6 Usage

Description

Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid, also known as norbornane-1-carboxylic acid, is a bicyclic organic compound with a unique molecular structure characterized by a fused bicyclic system. It is known for its stability and structural rigidity conferred by the norbornane framework, making it a valuable compound in various applications.

Uses

Used in Pharmaceutical Industry:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a starting material for the synthesis of various drugs and bioactive molecules due to its unique molecular structure and properties.
Used in Chemical Research:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a subject for studies in molecular modeling and stereochemistry, taking advantage of its conformational flexibility and stereochemical properties.
Used in Organic Synthesis:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a key intermediate in the synthesis of complex organic compounds, leveraging its stability and structural attributes for the development of novel chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 697-25-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 697-25:
(5*6)+(4*9)+(3*7)+(2*2)+(1*5)=96
96 % 10 = 6
So 697-25-6 is a valid CAS Registry Number.

697-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,6,7-hexahydrotricyclo[2.2.1.0<sup>2,6</sup>]heptane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names Nortricyclen-carbonsaeure-(1)

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:697-25-6 SDS

697-25-6Downstream Products

697-25-6Relevant articles and documents

Monoamine oxidase-catalyzed oxidation of endo,endo-2-amino-6-[(Z)-2'-phenyl]ethenylbicyclo[2.2.1]heptane, a potential probe for a radical cation intermediate

Wang, Xueqing,Silverman, Richard B.

, p. 1645 - 1651 (2007/10/03)

An 11-step synthesis of endo,endo-2-amino-6-[(E)-2'-phenyl]ethenylbicyclo[2.2.1]heptane (6) and the corresponding (Z)-isomer (7) was carried out in an attempt to make a compound that could trap the purported amine radical cation intermediate during monoamine oxidase (MAO)-catalyzed oxidation of amines. The E-isomer was not a substrate for MAO, and the Z-isomer was a very poor substrate. No trapping product was observed. Possible explanations for the inability of these compounds to trap a potential radical cation intermediate are discussed. Copyright (C) 2000 Elsevier Science Ltd.

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