825-03-6

Basic information

• Product Name: 2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID
• Synonyms: 5-METHYL-2-NORBORNENE-5-CARBOXYLIC ACID;2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID;2-METHYLBICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLIC ACID;TIMTEC-BB SBB008405
• CAS NO: 825-03-6
• Molecular Formula: C9H12O2
• Molecular Weight: 152.19
• Mol File: 825-03-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 80 °C
• Boiling Point: 261.352°C at 760 mmHg
• Flash Point: 121.096°C
• Appearance: /
• Vapor Pressure: 0.003mmHg at 25°C
• CAS DataBase Reference: 2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID(825-03-6)
• EPA Substance Registry System: 2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID(825-03-6)

Safety Data

• Hazard Codes: Xi:Irritant
• Statements: R36/37/38:Irritating to eyes, respiratory system and skin.
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39:Wear suitable g
• Hazardous Substances Data: 825-03-6(Hazardous Substances Data)

Usage

General Description

2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID is a chemical compound with a complex structure. It contains a bicyclic ring system, a double bond, a methyl group, and a carboxylic acid functional group. 2-METHYLBICYCLO[2.2.1]-5-HEPTENE-2-CARBOXYLIC ACID is likely to have a number of potential applications, including pharmaceuticals, agrochemicals, and materials science. Its structure suggests that it could have a variety of potential biological or chemical activities. However, further research and testing would be needed to determine its specific properties and potential uses.

InChI:InChI=1/C9H12O2/c1-9(8(10)11)5-6-2-3-7(9)4-6/h2-3,6-7H,4-5H2,1H3,(H,10,11)/p-1/t6-,7-,9-/m1/s1

Upstream product

• 79-41-4 poly(methacrylic acid) 
• 542-92-7 cyclopenta-1,3-diene 
• 40441-67-6 5-formyl-5-methylbicyclo[2.2.1]hept-2-ene 
• 77-73-6 bi(cyclopentadiene) 

Downstream Products

• 100869-68-9 (+/-)-5,6,7,8-tetrachloro-2-methyl-(4at,8at)-1,2,3,4,4a,5,8,8a-octahydro-1r,4c;5t,8t-dimethano-naphthalene-2ξ-carboxylic acid 
• 58055-94-0 ((1S,4S)-2-Methyl-bicyclo[2.2.1]hept-5-en-2-yl)-methanol 
• 91573-15-8 Toluene-4-sulfonic acid (1S,4S)-2-methyl-bicyclo[2.2.1]hept-5-en-2-ylmethyl ester 

Relevant articles and documents

Functional norbornanyl ester derivatives, polymers and process for preparing same

This invention relates to the new functional norbornanyl ester derivative and/or polymer compositions which are easily obtainable by reacting the Diels-Alder adduct of appropriate dienes and dienophiles with carboxylic acids. In particular, this invention relates to a new process for making cyclic chemical raw materials suitable for production coating, ink, adhesive, plasticizer, thermoplastic or thermosetting plastic and functional polymers.

Synthesis of a 1,3-spiro-amino-alcohol-derived chiral auxiliary and its application to Diels-Alder reactions

A short synthesis and resolution of (1R,5R,6R)-6-aminospiro[4.4]nonan-1-ol, 11, is reported. The pivalamide derivative (+)-5 gives excellent diastereo- and regiocontrol as well as endo selectivity as a chiral auxiliary in the BCl3-catalyzed Die

Acyloxyborane: An Activating Device for Carboxylic Acids

We chose α,β-unsaturated acids and investigated the reactivity of their borane adducts in Diels-Alder reactions.The reaction did proceed smoothly and has been found to be a useful method for synthesis of carboxylic acids.