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8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID, also known as 5,6,7,8-Tetrahydro-8-oxo-2-naphthoic Acid, is a chemical compound with potential therapeutic applications. It is characterized by its unique molecular structure, which includes a naphthalene core with a carboxylic acid group and an oxo group at the 8-position. 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID has been identified for its potential role in treating cancer and other Pin1-associated conditions.

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  • 89781-52-2 Structure
  • Basic information

    1. Product Name: 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID
    2. Synonyms: 8-oxo-6,7-dihydro-5H-naphthalene-2-carboxylic acid;5,6,7,8-tetrahydro-8-oxo-2-Naphthalenecarboxylic acid
    3. CAS NO:89781-52-2
    4. Molecular Formula: C11H10O3
    5. Molecular Weight: 190.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89781-52-2.mol
  • Chemical Properties

    1. Melting Point: 216 °C
    2. Boiling Point: 389.1±31.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.309±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 3.97±0.20(Predicted)
    10. CAS DataBase Reference: 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID(89781-52-2)
    12. EPA Substance Registry System: 8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID(89781-52-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 89781-52-2(Hazardous Substances Data)

89781-52-2 Usage

Uses

Used in Pharmaceutical Industry:
8-OXO-5,6,7,8-TETRAHYDRO-NAPHTHALENE-2-CARBOXYLIC ACID is used as a therapeutic agent for treating cancer and other Pin1-associated conditions. Its application is based on its ability to target and modulate the activity of Pin1, a peptidyl-prolyl isomerase enzyme that plays a crucial role in cell cycle regulation and has been implicated in the development and progression of various cancers. By inhibiting Pin1, this compound may help to prevent the growth and spread of cancer cells, offering a potential treatment option for patients with cancer and other Pin1-associated diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 89781-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89781-52:
(7*8)+(6*9)+(5*7)+(4*8)+(3*1)+(2*5)+(1*2)=192
192 % 10 = 2
So 89781-52-2 is a valid CAS Registry Number.

89781-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-oxo-6,7-dihydro-5H-naphthalene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 8-oxo-5,6,7,8-tetrahydronaphth-2-oic 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:89781-52-2 SDS

89781-52-2Relevant articles and documents

Diastereoselective. synergistic dual-mode optical switch with integrated chirochromic helicene and photochromic bis-azobenzene moieties

Chen, Wen-Ching,Lee, Yi-Wei,Chen, Chien-Tien

, p. 1472 - 1475 (2010)

(Figure Presented) An unprecedented dual-mode optical switch by combining helicene and bis-azobenzene moieties in proximity allows for cooperative, highly diastereoselective chlrochromic (92/8 to 3/97) and photochromic (>99/1 to 19/81) switchings both in

Radiolabeled platelet GPIIb/IIIa receptor antagonists as imaging agents for the diagnosis of thromboembolic disorders

-

, (2008/06/13)

This invention provides novel radiopharmaceuticals that are radiolabeled cyclic compounds containing carbocyclic or heterocyclic ring systems which act as antagonists of the platelet glycoprotein IIb/IIIa complex; to methods of using said radiopharmaceuticals as imaging agents for the diagnosis of arterial and venous thrombi; to novel reagents for the preparation of said radiopharmaceuticals; and to kits comprising said reagents.

Three novel mimics for the construction of sterically constrained protein turn models

Ernest,Kalvoda,Rihs,Mutter

, p. 4011 - 4014 (2007/10/02)

8-Amino-5,6,7,8-tetrahydro-2-naphthoic acid (1), 8-aminomethyl-5,6,7,8-tetrahydro-2-naphthoic acid (2), and 8-aminomethyl-2-naphthoic acid (3) were synthesized in their protected forms for use in the construction of sterically constrained protein turn models.

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