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CAS

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102296-44-6

1-(1,1-dimethylindan-5-yl)ethanone, also known as P55, is a unique chemical compound belonging to the ketone family. It features a distinctive molecular structure with a substituent at the 5-position of the indane ring, which contributes to its potential reactivity and interesting properties. 1-(1,1-dimethylindan-5-yl)ethanone has garnered attention for its possible applications in various fields, including pharmaceuticals, organic synthesis, and even as a flavoring agent or fragrance due to its aromatic characteristics. Further research is essential to explore and confirm the full spectrum of uses and properties of 1-(1,1-dimethylindan-5-yl)ethanone.

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  • 102296-44-6 Structure

  • Basic information

    1. Product Name: 1-(1,1-dimethylindan-5-yl)ethanone
    2. Synonyms: 1-(1,1-Dimethyl-2,3-dihydro-1H-inden-5-yl)ethanone; ethanone, 1-(2,3-dihydro-1,1-dimethyl-1H-inden-5-yl)-
    3. CAS NO:102296-44-6
    4. Molecular Formula: C13H16O
    5. Molecular Weight: 188.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102296-44-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 292.2°C at 760 mmHg
    3. Flash Point: 121.3°C
    4. Appearance: N/A
    5. Density: 0.998g/cm3
    6. Vapor Pressure: 0.00186mmHg at 25°C
    7. Refractive Index: 1.525
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(1,1-dimethylindan-5-yl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(1,1-dimethylindan-5-yl)ethanone(102296-44-6)
    12. EPA Substance Registry System: 1-(1,1-dimethylindan-5-yl)ethanone(102296-44-6)

  • 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: 102296-44-6(Hazardous Substances Data)

102296-44-6 Usage

Uses

Used in Pharmaceutical Applications:
1-(1,1-dimethylindan-5-yl)ethanone is used as a compound in pharmaceutical research for its potential reactivity and unique molecular structure, which may contribute to the development of new drugs and therapies.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(1,1-dimethylindan-5-yl)ethanone is used as a key intermediate or building block for the creation of more complex molecules and compounds, thanks to its specific structural features.
Used in Flavor and Fragrance Industry:
1-(1,1-dimethylindan-5-yl)ethanone is used as a potential flavoring agent or fragrance component due to its aromatic properties, which could be harnessed to create novel scents and tastes in the industry.

Check Digit Verification of cas no

The CAS Registry Mumber 102296-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,9 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102296-44:
(8*1)+(7*0)+(6*2)+(5*2)+(4*9)+(3*6)+(2*4)+(1*4)=96
96 % 10 = 6
So 102296-44-6 is a valid CAS Registry Number.

102296-44-6SDS

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 1-(1,1-dimethyl-2,3-dihydroinden-5-yl)ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-(2,3-dihydro-1,1-dimethyl-1H-inden-5-yl)

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:102296-44-6 SDS

102296-44-6Downstream Products

102296-44-6Relevant articles and documents

STRUCTURE OF THE SIDE PRODUCTS IN THE SYNTHESIS OF 4-ACETYL-1,1-DIMETHYL-6-TERT-BUTYLINDANE

Smirnova, O. B.,Cherkaev, G. V.,Shekhtman, N. M.

, p. 2123 - 2127 (2007/10/02)

The minor products from the acetylation of 1,1-dimethyl-6-tert-butylindane with acetyl chloride were isolated and identified by PMR spectroscopy.The configuration of the substituents in isomeric compounds with an identical type of substitution in the aromatic ring was established by means of the long-range spin-spin coupling constants of the aromatic protons with the protons of the five-membered ring.

The Stereochemistry of Organometallic Compounds. XXVII. Nucleophilic and Electrophilic Substitution Reactions of Conformationally Restricted Arenechromium Compounds

Jackson, W. Roy,Rae, Ian D.,Wong, Margaret G.

, p. 303 - 315 (2007/10/02)

The regioselectivity of reaction of tricarbonyl(1,1-dimethylindane)chromium with selected electrophiles and nucleophiles has been shown to be influenced by the preferred conformation of the tricarbonylchromium group.Nucleophiles preferentially react at carbon atoms eclipsed by a chromium-carbonyl bond and electrophiles at carbon atoms in staggered positions.When similar reactions were attempted with some chelated arenechromium dicarbonyl phosphorus compounds only low yields of substitution products were obtained.

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