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CAS

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173156-86-0

4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 173156-86-0 Structure

  • Basic information

    1. Product Name: 4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid
    2. Synonyms: 4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid
    3. CAS NO:173156-86-0
    4. Molecular Formula: C21H24O2S
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173156-86-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 506.5°Cat760mmHg
    3. Flash Point: 260.1°C
    4. Appearance: /
    5. Density: 1.18g/cm3
    6. Vapor Pressure: 4.41E-11mmHg at 25°C
    7. Refractive Index: 1.621
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid(173156-86-0)
    12. EPA Substance Registry System: 4-(5,5,8,8-tetramethyltetralin-2-yl)sulfanylbenzoic acid(173156-86-0)

  • 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: 173156-86-0(Hazardous Substances Data)

173156-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173156-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,1,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 173156-86:
(8*1)+(7*7)+(6*3)+(5*1)+(4*5)+(3*6)+(2*8)+(1*6)=140
140 % 10 = 0
So 173156-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H24O2S/c1-20(2)11-12-21(3,4)18-13-16(9-10-17(18)20)24-15-7-5-14(6-8-15)19(22)23/h5-10,13H,11-12H2,1-4H3,(H,22,23)

173156-86-0SDS

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 4-[(5,5,8,8-tetramethyl-1,2,3,4-tetrahydronaphthalen-2-yl)sulfanyl]benzoic 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:173156-86-0 SDS

173156-86-0Downstream Products

173156-86-0Relevant articles and documents

Composition containing at least one bicyclic aromatic compound and at least one lipophilic sunscreen, and uses thereof

-

, (2008/06/13)

A composition containing at least one lipophilic sunscreen and at least one bicyclic aromatic compound represented by formula (I): or a salt or chiral analogue of such a compound, where the structural variables R1, Ar, X, R2 Y and X are defined herein, and at least one lipophilic sunscreen.

RXR-agonist polycyclic aromatic compounds, pharmaceutical/cosmetic compositions comprising said compound and uses thereof

-

, (2008/06/13)

Novel pharmaceutically/cosmetically-active polycyclic aromatic compounds having the structural formula (I): wherein Ar is a radical having one of the formulae (a)-(e): which are useful for the treatment of a wide variety of disease states, whether human or veterinary, for example dermatological, rheumatic, respiratory, cardiovascular and ophthalmological disorders, as well as for the treatment of mammalian skin and hair conditions/disorders are provided. In particular, based on their RXR-agonist activity, these compounds may be used to treat noninsulin-dependent diabetes mellitus (NIDDM) and obesity.

Synthesis and structure-activity relationships of retinoid X receptor selective diaryl sulfide analogs of retinoic acid

Beard, Richard L.,Colon, Diana F.,Song, Tae K.,Davies, Peter J. A.,Kochhar, Devendra M.,Chandraratna, Roshantha A. S.

, p. 3556 - 3563 (2007/10/03)

Retinoids exert their biological effects by binding to and activating nuclear receptors that interact with responsive elements on DNA to promote gene transcription. There are two families of retinoid receptors, the retinoic acid receptor (RAR) family and

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