What is the 2,3-NORBORNANEDICARBOXYLIC ACID?

2,3-NORBORNANEDICARBOXYLIC ACID is , while it's Molecular Formula is C 9 H 12 O 4 . Used in Organic Synthesis: 2,3-Norbornanedicarboxylic Acid is used as a reagent for the preparation of certain polymers. Its unique structure and properties make it a valuable component in the synthesis of various organic compounds. Used in Polymer Preparation: 2,3-Norbornanedicarboxylic Acid is used as a key ingredient in the production of specific polymers. Its dicarboxylic acid nature allows it to form ester linkages, contributing to the structural integrity and properties of the resulting polymers. Used in Chemical Research: 2,3-Norbornanedicarboxylic Acid is used as a research compound in the field of chemistry. Its unique structure and reactivity make it an interesting subject for studies on organic synthesis, polymer chemistry, and material science. Safety Considerations: When handling 2,3-Norbornanedicarboxylic Acid, it is important to be aware of its potential hazards, such as the generation of toxic gases or vapours when heated. Protective measures, including proper ventilation and personal protective equipment, are advised to ensure safe handling and use of this chemical.

What is the CAS number for 2,3-NORBORNANEDICARBOXYLIC ACID?

The CAS number of 2,3-NORBORNANEDICARBOXYLIC ACID is 1724-08-9.

What is the 2,3-NORBORNANEDICARBOXYLIC ACID?

2,3-NORBORNANEDICARBOXYLIC ACID is , while it's Molecular Formula is C 9 H 12 O 4 . Used in Organic Synthesis: 2,3-Norbornanedicarboxylic Acid is used as a reagent for the preparation of certain polymers. Its unique structure and properties make it a valuable component in the synthesis of various organic compounds. Used in Polymer Preparation: 2,3-Norbornanedicarboxylic Acid is used as a key ingredient in the production of specific polymers. Its dicarboxylic acid nature allows it to form ester linkages, contributing to the structural integrity and properties of the resulting polymers. Used in Chemical Research: 2,3-Norbornanedicarboxylic Acid is used as a research compound in the field of chemistry. Its unique structure and reactivity make it an interesting subject for studies on organic synthesis, polymer chemistry, and material science. Safety Considerations: When handling 2,3-Norbornanedicarboxylic Acid, it is important to be aware of its potential hazards, such as the generation of toxic gases or vapours when heated. Protective measures, including proper ventilation and personal protective equipment, are advised to ensure safe handling and use of this chemical.

What is the CAS number for 2,3-NORBORNANEDICARBOXYLIC ACID?

The CAS number of 2,3-NORBORNANEDICARBOXYLIC ACID is 1724-08-9.

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1724-08-9

Product Name：2,3-Norbornanedicarboxylic Acid
Molecular Formula：C9H12 O4
Purity：99%
Molecular Weight：184.192

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Product Details;

CasNo： 1724-08-9

Molecular Formula： C9H12 O4

factory and supplier 1724-08-9 2,3-Norbornanedicarboxylic Acid in stock

Molecular Formula:C₉H₁₂O₄
Molecular Weight:184.192
Vapor Pressure:8.65E-08mmHg at 25°C
Melting Point:150 °C(Solv: acetic acid (64-19-7))
Boiling Point:407.7°Cat760mmHg
PKA:4.12±0.40(Predicted)
Flash Point:214.5°C
PSA：74.60000
Density:1.42g/cm³
LogP:0.81790

2,3-NORBORNANEDICARBOXYLIC ACID(Cas 1724-08-9) Usage

General Description

2,3-Norbornanedicarboxylic Acid, also known as Cyclic-2.3.-(1,2:3,4-diepoxybutane)-1,4.5.6-tetrahydrophthalic acid or endo-cis-5-Norbornene-endo-2,3-dicarboxylic acid, is an organic compound and a dicarboxylic acid with the molecular formula C9H10O4. This technical-grade chemical appears as white crystals and has a mild odour. It is used as a reagent in organic synthesis, particularly in the preparation of certain polymers. With an estimated melting point of 165-167 °C, it has potential hazards such as the generation of toxic gases or vapours when heated. Therefore, protective measures are advised when handling it.

InChI:InChI=1/C9H12O4/c10-8(11)6-4-1-2-5(3-4)7(6)9(12)13/h4-7H,1-3H2,(H,10,11)(H,12,13)

1724-08-9 Relevant articles

-

Wilder,Winston

, p. 868,870 (1956)

Optical Resolution of trans-Bicycloheptane-2,3-diamine: Chiral Recognition in the Crystal of its Complex with (2R,3R)-O,O'-Dibenzoyltartaric Acid

Hatano, Keiichiro,Takeda, Tadahiro,Saito, Reiko

, p. 579 - 584 (2007/10/02)

The synthesis of trans-bicycloheptane-2,...

Electrochemical incorporation of carbon dioxide into alkenes by nickel complexes

Derien, Sylvie,Clinet, Jean-Claude,Dunach, Elisabet,Perichon, Jacques

, p. 5235 - 5248 (2007/10/02)

Electrogenerated Ni(0) complexes from st...

Chiral rhodium-diphosphine catalyst capable of catalytic reduction of a tetramisole precursor to give a significant excess of the desired S-(-)isomer, levamisole

-

, (2008/06/13)

A soluble, chiral, rhodium-containing ca...

1724-08-9 Process route

: 3014-58-2,5826-73-3,7184-07-8,39589-98-5,116404-47-8,117604-28-1,135357-64-1
dimethyl (exo,endo)-bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate

: 1724-08-9,2435-37-2,6343-11-9,27862-85-7,58616-96-9,58616-98-1,70095-10-2
(+/-)-norbornane-2endo,3exo-dicarboxylic acid

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: NaOMe, water / methanol / 1.5 h / Heating 2: 100 percent / H₂ / Rh-Pd/C With water; hydrogen; sodium methylate; Rh-Pd on carbon; In methanol;
Multi-step reaction with 2 steps 1: ethanol; palladium/barium sulfate / Hydrogenation 2: ethanolic KOH-solution With potassium hydroxide; Pd-BaSO₄; ethanol;