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1623-09-2

6-tert-butyl-2,3-dihydro-1H-inden-5-ol is a chemical compound with the molecular formula C14H22O. It is a white crystalline solid that belongs to the class of organic compounds known as indenols. 6-tert-butyl-2,3-dihydro-1H-inden-5-ol is characterized by a five-membered aromatic ring with a hydroxyl group at the 5-position, a 2,3-dihydro structure, and a tert-butyl group at the 6-position. It is synthesized through various chemical reactions and is used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits specific chemical properties and reactivity, making it a valuable intermediate in the synthesis of various complex organic molecules.

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  • 1623-09-2 Structure

  • Basic information

    1. Product Name: 6-tert-butyl-2,3-dihydro-1H-inden-5-ol
    2. Synonyms:
    3. CAS NO:1623-09-2
    4. Molecular Formula: C13H18O
    5. Molecular Weight: 190.2814
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1623-09-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 284.1°C at 760 mmHg
    3. Flash Point: 127.8°C
    4. Appearance: N/A
    5. Density: 1.036g/cm3
    6. Vapor Pressure: 0.00177mmHg at 25°C
    7. Refractive Index: 1.552
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-tert-butyl-2,3-dihydro-1H-inden-5-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-tert-butyl-2,3-dihydro-1H-inden-5-ol(1623-09-2)
    12. EPA Substance Registry System: 6-tert-butyl-2,3-dihydro-1H-inden-5-ol(1623-09-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1623-09-2(Hazardous Substances Data)

1623-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1623-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1623-09:
(6*1)+(5*6)+(4*2)+(3*3)+(2*0)+(1*9)=62
62 % 10 = 2
So 1623-09-2 is a valid CAS Registry Number.

1623-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-tert-butyl-indan-5-ol

1.2 Other means of identification

Product number -
Other names 6-tert.-Butylindanol-(5)

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:1623-09-2 SDS

1623-09-2Relevant articles and documents

Catalyst components for the polymerization of olefins

-

Page/Page column, (2014/12/09)

A solid catalyst component for the polymerization of olefins comprising Mg, Ti, Cl and at least an electron donor compound which is the reaction product obtained by bringing into contact a Mg compound and a Ti compound having at least a Ti-halogen bond with an electron donor selected from specific diphenol derivatives.

4-Hydroxy-5,6-dihydro-2H-pyran-2-ones. 3. Bicyclic and hetero-aromatic ring systems as 3-position scaffolds to bind to S1' and S1' of the HIV-1 protease enzyme

Ellsworth, Edmund L.,Domagala, John,Vara Prasad,Hagen, Susan,Ferguson, Donna,Holler, Tod,Hupe, Donald,Graham, Neil,Nouhan, Caroline,Tummino, Peter J.,Zeikus, Greg,Lunney, Elizabeth A.

, p. 2019 - 2024 (2007/10/03)

56-Dihydro-2H-pyran-2-ones are potent inhibitors of HIV-1 protease which bind to the S1 S2 S1' S2' pockets have a unique binding mode with the catalytic aspartyl groups the flap region of the enzyme. Efforts to explore 3-position heterocyclic scaffolds that bind to the S1' S2' pockets have provided a number of selected analogs that display high HIV-1 protease inhibitory activity.

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