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23357-47-3

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23357-47-3 Usage

Description

(R)-1,2,3,4-Tetrahedro-naphthoic acid, also known as Tetrahydronaphthoic acid, is a versatile organic compound with a unique tetrahedral structure derived from naphthalene. It possesses acidic properties and is characterized by its four fused rings, which contribute to its stability and reactivity. (R)-1,2,3,4-Tetrahedro-naphthoic acid is widely utilized in the pharmaceutical and chemical industries due to its diverse applications and potential for further chemical modifications.

Uses

Used in Pharmaceutical Industry:
(R)-1,2,3,4-Tetrahedro-naphthoic acid is used as an intermediate in the preparation of Dipeptidyl Boronate Proteasome Inhibitors. These inhibitors play a crucial role in the development of drugs targeting various diseases, including cancer, by disrupting the function of proteasomes, which are essential for protein degradation and cellular regulation.
(R)-1,2,3,4-Tetrahedro-naphthoic acid is also used as a palonosetron intermediate. Palonosetron is a selective 5-HT3 receptor antagonist used to treat nausea and vomiting associated with chemotherapy. The compound's unique structure allows for the development of more effective and targeted pharmaceutical agents.
Used in Chemical Industry:
(R)-1,2,3,4-Tetrahedro-naphthoic acid is used for the construction of sterically constrained protein turn models. These models are essential in understanding protein folding and function, which can lead to the development of new drugs and therapies for various diseases. The compound's rigid structure and chemical properties make it an ideal candidate for creating these models and furthering our understanding of protein dynamics.

Check Digit Verification of cas no

The CAS Registry Mumber 23357-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,5 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23357-47:
(7*2)+(6*3)+(5*3)+(4*5)+(3*7)+(2*4)+(1*7)=103
103 % 10 = 3
So 23357-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7H2,(H,12,13)/t10-/m1/s1

23357-47-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H27673)  (R)-1,2,3,4-Tetrahydro-1-naphthoic acid, 98%   

  • 23357-47-3

  • 250mg

  • 831.0CNY

  • Detail
  • Alfa Aesar

  • (H27673)  (R)-1,2,3,4-Tetrahydro-1-naphthoic acid, 98%   

  • 23357-47-3

  • 1g

  • 2130.0CNY

  • Detail
  • Alfa Aesar

  • (H27673)  (R)-1,2,3,4-Tetrahydro-1-naphthoic acid, 98%   

  • 23357-47-3

  • 5g

  • 7363.0CNY

  • Detail

23357-47-3SDS

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 (1R)-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names (R)-1,2,3,4-Tetrahydro-1-naphthoic acid

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:23357-47-3 SDS

23357-47-3Relevant articles and documents

Method for preparing (S)-tetrahydro-1-naphthoic acid through high-efficiency resolution

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Paragraph 0006; 0015; 0017, (2018/03/13)

The invention relates to a preparation method of a palonosetron hydrochloride key intermediate (S)-1,2,3,4-tetrahydro-1-naphthoic acid as shown in a formula (I). The method comprises the following steps of adding a resolution agent for resolution by adopting 1,2,3,4-tetrahydro-naphthalene acid racemate as a raw material to obtain a salt (III) formed by a (S)-1,2,3,4-tetrahydro naphthalene acid and the resolution agent, and a salt (IV) formed by (R)-1,2,3,4-tetrahydro naphthalene acid and the resolution agent; carrying out salt removing on a compound III and a compound IV separately to obtain compounds (I) and (II); and carrying out racemization on the compound (II) under an alkaline condition to obtain a starting material 1,2,3,4-tetrahydro-naphthalene acid racemate and further carrying out resolution according to the steps. Therefore, the overall yield can be greatly improved, the production cost is reduced and environmental protection is facilitated. The preparation technology of the palonosetron hydrochloride key intermediate provided by the invention is different from the prior art, is safe, environmentally friendly, simple in operation and high in yield, and has relatively great practical value. The formula is as shown in the specification.

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