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838-03-9

1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone is a complex organic compound with the molecular formula C14H14O4. It is characterized by a naphthalene ring structure, which consists of two fused benzene rings, with two methyl groups attached at the 3rd and 6th positions. The compound features two hydroxyl groups at the 1st and 8th positions, and a carbonyl group (C=O) attached to the 2nd position of the naphthalene ring. This carbonyl group is connected to an ethanone (CH3-CH2-C=O) side chain, which extends from the naphthalene core. The compound is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of dyes and other organic compounds. Its unique structure and functional groups make it an interesting target for further research and development in the field of organic chemistry.

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  • 838-03-9 Structure

  • Basic information

    1. Product Name: 1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone
    2. Synonyms: 1-(1,8-dihydroxy-3,6-dimethyl-2-naphthyl)ethan-1-one; 2-acetyl-1,8-dihydroxy-3,6-dimethylnaphthalene; Naphthalene-1,8-diol, 2-acetyl-3,6-dimethyl-
    3. CAS NO:838-03-9
    4. Molecular Formula: C14H14O3
    5. Molecular Weight: 230.2592
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 838-03-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 426.9°C at 760 mmHg
    3. Flash Point: 226.1°C
    4. Appearance: N/A
    5. Density: 1.248g/cm3
    6. Vapor Pressure: 6.86E-08mmHg at 25°C
    7. Refractive Index: 1.652
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone(838-03-9)
    12. EPA Substance Registry System: 1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone(838-03-9)

  • 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: 838-03-9(Hazardous Substances Data)

838-03-9 Usage

Chemical family

Aromatic ketones

Physical state

Yellow crystalline solid

Molecular weight

230.26 g/mol

Uses

a. Synthesis of pharmaceuticals and organic compounds
b. Flavoring agent in the food industry
c. Fragrance in the cosmetics industry

Properties

a. Aromatic nature
b. Ketone functionality
c. Antioxidant properties

Potential applications

Development of antioxidant therapies

Check Digit Verification of cas no

The CAS Registry Mumber 838-03-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 838-03:
(5*8)+(4*3)+(3*8)+(2*0)+(1*3)=79
79 % 10 = 9
So 838-03-9 is a valid CAS Registry Number.

838-03-9SDS

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 1-(1,8-dihydroxy-3,6-dimethylnaphthalen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1',8'-dihydroxy-3',6'-dimethyl-2'-acetonaphthone

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:838-03-9 SDS

838-03-9Relevant articles and documents

Total synthesis of the antifungal natural product mollisin

Schwolow, Sonja,Kunz, Horst,Rheinheimer, Joachim,Opatz, Till

, p. 6519 - 6524 (2013)

Mollisin, a bioactive polyketide secondary metabolite of the fungus Mollisia caesia, was synthesized in nine linear steps from commercially available 2,6-dimethyl-γ-pyrone. A key transformation in this first total synthesis of mollisin was the ipso substi

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