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32229-19-9

Benzene, 2-bromo-1-methoxy-4-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 32229-19-9 Structure

  • Basic information

    1. Product Name: Benzene, 2-bromo-1-methoxy-4-(1-methylethyl)-
    2. Synonyms:
    3. CAS NO:32229-19-9
    4. Molecular Formula: C10H13BrO
    5. Molecular Weight: 229.117
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 32229-19-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzene, 2-bromo-1-methoxy-4-(1-methylethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 2-bromo-1-methoxy-4-(1-methylethyl)-(32229-19-9)
    11. EPA Substance Registry System: Benzene, 2-bromo-1-methoxy-4-(1-methylethyl)-(32229-19-9)

  • 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: 32229-19-9(Hazardous Substances Data)

32229-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32229-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,2 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32229-19:
(7*3)+(6*2)+(5*2)+(4*2)+(3*9)+(2*1)+(1*9)=89
89 % 10 = 9
So 32229-19-9 is a valid CAS Registry Number.

32229-19-9Relevant articles and documents

Bromination of Anisoles Using N-Bromophthalimide: A Synthetic and Kinetic Approach

Anjaiah,Kumar, M. Satish,Srinivas,Rajanna

, p. 98 - 105 (2016)

N-Bromophthalimide (NBP)-triggered bromination of aromatic compounds has been studied in the presence of aqueous acetic acid. Reaction Kinetics indicated first order in [NBP] and zero order in [Anisole]. The reactions afforded very good yields of corresponding bromo derivatives under kinetic conditions. The mechanism of the reaction is explained through the formation of acetyl hypobromite due to the interaction of NBP and acetic acid, which in turn reacts with anisole to afford a bromo derivative of anisole.

Tropos deoxycholic acid-derived biphenylphosphites: synthesis, stereochemical characterization and use as chiral ligands in the copper catalyzed conjugate addition of diethylzinc to acyclic enones

Facchetti, Sarah,Losi, Debora,Iuliano, Anna

, p. 2993 - 3003 (2007/10/03)

Three new deoxycholic acid-based 5,5′-substituted biphenylphosphites, 2-4, were synthesized and their stereochemical features were examined by CD and NMR spectroscopy, which allowed us to determine the sense of twist of the substituted biphenyl moiety as

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