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CAS

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42036-59-9

1-(6-chloronaphthalen-2-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 42036-59-9 Structure

  • Basic information

    1. Product Name: 1-(6-chloronaphthalen-2-yl)ethanone
    2. Synonyms: 1-(6-Chloro-2-naphthyl)ethanone
    3. CAS NO:42036-59-9
    4. Molecular Formula: C12H9ClO
    5. Molecular Weight: 204.6523
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 42036-59-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 337°C at 760 mmHg
    3. Flash Point: 170.8°C
    4. Appearance: N/A
    5. Density: 1.225g/cm3
    6. Vapor Pressure: 0.000108mmHg at 25°C
    7. Refractive Index: 1.624
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(6-chloronaphthalen-2-yl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(6-chloronaphthalen-2-yl)ethanone(42036-59-9)
    12. EPA Substance Registry System: 1-(6-chloronaphthalen-2-yl)ethanone(42036-59-9)

  • 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: 42036-59-9(Hazardous Substances Data)

42036-59-9 Usage

Type of compound

Ketone

Derived from

Naphthalene

Contains

Chlorine atom

Common uses

a. Organic synthesis
b. Intermediate in the production of pharmaceuticals
c. Intermediate in the production of dyes
d. Intermediate in the production of other chemical compounds

Known for

a. Potential use as a reagent in chemical reactions
b. Structure and properties useful in various industrial applications

Ongoing research and development

Potential uses in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 42036-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,3 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42036-59:
(7*4)+(6*2)+(5*0)+(4*3)+(3*6)+(2*5)+(1*9)=89
89 % 10 = 9
So 42036-59-9 is a valid CAS Registry Number.

42036-59-9Relevant articles and documents

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

, (2021/01/22)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

, (2019/07/17)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

Sequential Acetalization-Pyrolysis of α-Acetylcinnamates and α-Acetylbenzalacetones. A Method for the Generation of 2-Carbonyl-Subsituted Naphthalenes

Zoeller, Joseph R.,Sumner, Charles E.

, p. 319 - 324 (2007/10/02)

Substituted 2-acetonaphthones and 2-naphthoate methyl esters can be generated from benzaldehydes in a sequence of three reaction steps.Knoevenagel condensation of a benzaldehyde with 2,4-pentandione of methyl acetoacetate yields α-carbonyl-substituted benzalacetones.The α-carbonyl-substituted benzalacetones are then cyclized to generate the α-carbonyl-substituted naphthalenes by a sequential acetalization with trimethyl orthoformate followed by subsequent pyrolysis of the dimethyl acetal either in the vapor phase at 475 deg C or by being heated in boiling 1-methylnaphthalene. 2-Acetonaphthones are obtained when 2,4-pentanedione is used and 2-naphthoate methyl esters are obtained from methyl acetoacetate.

SEQUENTIAL ACETALIZATION-PYROLYSIS OF α-ACETYL BENZALACETONES. A METHOD FOR THE GENERATION OF 6-SUBSTITUTED 2-ACETONAPHTHONES

Zoeller, Joseph R.

, p. 1457 - 1460 (2007/10/02)

6-Substituted 2-acetonaphthones can be generated from para substituted benzaldehydes and acetylacetone (2,4-pentanedione) in three reactions consisting of condensing the benzaldehyde with acetylacetone, acetalizing the resultant 3-benzylidene 2,4-pentanedione (α-acetyl benzalacetones), with trimethyl orthoformate, pyrolyzing the acetal either in the vapor phase at 475 deg C or by heating in a high boiling solvent, such as 1-methylnaphthalene.

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