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83037-99-4

5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83037-99-4 Structure

  • Basic information

    1. Product Name: 5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE
    2. Synonyms: 5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE
    3. CAS NO:83037-99-4
    4. Molecular Formula: C10H13BrO
    5. Molecular Weight: 229.11
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83037-99-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 266.7±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.305±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE(83037-99-4)
    11. EPA Substance Registry System: 5-(BROMOMETHYL)-2-METHOXY-1,3-DIMETHYLBENZENE(83037-99-4)

  • 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: 83037-99-4(Hazardous Substances Data)

83037-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83037-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,3 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83037-99:
(7*8)+(6*3)+(5*0)+(4*3)+(3*7)+(2*9)+(1*9)=134
134 % 10 = 4
So 83037-99-4 is a valid CAS Registry Number.

83037-99-4Downstream Products

83037-99-4Relevant articles and documents

Visible-Light-Induced Cyclization of Electron-Enriched Phenyl Benzyl Sulfides: Synthesis of Tetrahydrofurans and Tetrahydropyrans

Li, Wei,Yang, Chao,Gao, Guo-Lin,Xia, Wujiong

supporting information, p. 1391 - 1396 (2016/06/01)

A new approach to the preparation of tetrahydrofurans and tetrahydropyrans through a photoredox catalytic process is described. The introduction of a phenylsulfanyl auxiliary group permits the substrates to be readily oxidized to form cationic intermediates for sequential intramolecular cyclization. The method features mild reaction conditions and operational simplicity.

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