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(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, commonly referred to as norbornene-2-carboxylic acid, is a bicyclic organic compound characterized by its carboxylic acid functional group. It is derived from norbornene, a bicyclic hydrocarbon, and is recognized for its distinctive structure and reactivity. (1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid serves as a crucial building block in organic synthesis, particularly in the creation of pharmaceuticals, agrochemicals, and fine chemicals. Its potential extends to polymer science, where it is utilized to synthesize polymers with tailored properties and characteristics. Moreover, it has been explored for its applications in catalysis and as a ligand in organometallic chemistry.

934-30-5

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934-30-5 Usage

Uses

Used in Pharmaceutical Industry:
(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique reactivity and structural features, which allow for the development of complex molecular architectures with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, (1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is employed as a precursor for the production of agrochemicals, leveraging its chemical properties to create compounds that can be used in pest control and crop protection.
Used in Fine Chemicals Production:
(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is utilized as a building block in the synthesis of fine chemicals, where its unique structure contributes to the creation of high-value specialty chemicals for various applications.
Used in Polymer Science:
(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is used as a monomer in polymer synthesis to produce polymers with specific properties, such as thermal stability, mechanical strength, or chemical resistance, tailored for use in various industries.
Used in Catalysis:
(1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid has potential applications in catalysis, where it may serve to enhance the efficiency of chemical reactions, potentially leading to more sustainable and cost-effective processes in the chemical industry.
Used in Organometallic Chemistry:
As a ligand in organometallic chemistry, (1R,2S,4R)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid contributes to the development of novel catalysts and organometallic complexes, which are valuable in various chemical transformations and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 934-30-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934-30:
(5*9)+(4*3)+(3*4)+(2*3)+(1*0)=75
75 % 10 = 5
So 934-30-5 is a valid CAS Registry Number.

934-30-5 Well-known Company Product Price

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  • Aldrich

  • (718149)  exo-5-Norbornenecarboxylicacid  97%

  • 934-30-5

  • 718149-1G

  • 1,062.36CNY

  • Detail
  • Aldrich

  • (718149)  exo-5-Norbornenecarboxylicacid  97%

  • 934-30-5

  • 718149-5G

  • 3,521.70CNY

  • Detail

934-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name exo-5-Norbornene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:934-30-5 SDS

934-30-5Relevant academic research and scientific papers

The design and synthesis of novel adenosine agonists

Scammells,Baker,Bellardinelli,Olsson,Russell,Knevitt

, p. 811 - 814 (1996)

The 2R and 2S-endo isomers of N6-(5,6-epoxynorborn-2-yl)adenosine have been synthesised and shown to be potent agonists for the A1 adenosine receptor. The 2S-endo isomer was equipotent to N6-cyclopentyladenosine and 10- to 12-fold more potent than the 2R-endo isomer.

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