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1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174967-28-3 Structure
  • Basic information

    1. Product Name: 1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE
    2. Synonyms: 1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE
    3. CAS NO:174967-28-3
    4. Molecular Formula: C16H13Br
    5. Molecular Weight: 285.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174967-28-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE(174967-28-3)
    11. EPA Substance Registry System: 1-BROMO-3-(4-PHENYL-1,3-BUTADIENYL)BENZENE(174967-28-3)
  • 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: 174967-28-3(Hazardous Substances Data)

174967-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174967-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174967-28:
(8*1)+(7*7)+(6*4)+(5*9)+(4*6)+(3*7)+(2*2)+(1*8)=183
183 % 10 = 3
So 174967-28-3 is a valid CAS Registry Number.

174967-28-3Downstream Products

174967-28-3Relevant articles and documents

Indium triflate catalyzed rearrangement of aryl-substituted cyclopropyl carbinols to 1,4-disubstituted 1,3-butadienes

Ranu, Brindaban C.,Banerjee, Subhash

, p. 3012 - 3015 (2007/10/03)

Aryl-substituted cyclopropyl carbinol derivatives undergo a facile stereoselective rearrangement catalyzed by In(OTf)3 in dichloromethane under sonication to produce the substituted conjugated all-trans-butadienes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Catalysis by ionic liquids: Cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions

Ranu, Brindaban C.,Banerjee, Subhash,Das, Arijit

, p. 881 - 884 (2007/10/03)

Aryl substituted cyclopropyl carbinol derivatives undergo stereoselective rearrangements catalyzed by the ionic liquid, 1-methyl-3-pentylimidazolium bromide, under sonication, without any organic solvent, to produce the substituted conjugated all-trans-butadienes.

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