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1,2-dichloro-3,5-dimethylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75487-12-6 Structure
  • Basic information

    1. Product Name: 1,2-dichloro-3,5-dimethylbenzene
    2. Synonyms: 1,2-Dichloro-3,5-dimethylbenzene; benzene, 1,2-dichloro-3,5-dimethyl-
    3. CAS NO:75487-12-6
    4. Molecular Formula: C8H8Cl2
    5. Molecular Weight: 175.0551
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75487-12-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 229.8°C at 760 mmHg
    3. Flash Point: 92.2°C
    4. Appearance: N/A
    5. Density: 1.199g/cm3
    6. Vapor Pressure: 0.103mmHg at 25°C
    7. Refractive Index: 1.538
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2-dichloro-3,5-dimethylbenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-dichloro-3,5-dimethylbenzene(75487-12-6)
    12. EPA Substance Registry System: 1,2-dichloro-3,5-dimethylbenzene(75487-12-6)
  • 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: 75487-12-6(Hazardous Substances Data)

75487-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75487-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,8 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75487-12:
(7*7)+(6*5)+(5*4)+(4*8)+(3*7)+(2*1)+(1*2)=156
156 % 10 = 6
So 75487-12-6 is a valid CAS Registry Number.

75487-12-6Downstream Products

75487-12-6Relevant articles and documents

Photoadducts of 4,6-Dimethyl- and 4-Methoxy-6-methyl-2-pyrones with Chloroethylenes and Their Dehydrochlorination

Shimo, Tetsuro,Somekawa, Kenichi,Wakikawa, Yusuke,Uemura, Hisako,Tsuge, Otohiko,et al.

, p. 621 - 626 (2007/10/02)

Sensitized photoreactions of 2-pyrones with chloroethylenes gave two kinds of cycloadducts, 2-oxabicyclooct-4-en-3-ones (4,8) and across the C3-C4 double bond in 2-pyrone, benzene derivatives, and/or cyclobutanecarboxylic acids: Their relative yields greatly depended upon the nature of the reactants.The dehydrochlorination of the cycloadducts 4 and 8 across the C5-C6 double bonds in the pyrones with triethylamine in ethanol gave 5-ethenyl-2-pyrones, whose structures were previously incorrectly assigned as oxocinones, via a symmetry-allowed ring opening of 2-oxabicycloocta-4,6-dien-3-ones.Some 5-ethenyl-2-pyrones possessing a chlorinated ethenyl group finally affords 5-ethynyl-2-pyrones by an anti-elimination of hydrogen chloride.The X-ray crystallographic analyses of 5-ethenyl- and 5-ethynyl-2-pyrones are also described.

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