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(E)-1-bromo-3-(4-methylstyryl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 226712-71-6 Structure
  • Basic information

    1. Product Name: (E)-1-bromo-3-(4-methylstyryl)benzene
    2. Synonyms: (E)-1-bromo-3-(4-methylstyryl)benzene
    3. CAS NO:226712-71-6
    4. Molecular Formula:
    5. Molecular Weight: 273.172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 226712-71-6.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: (E)-1-bromo-3-(4-methylstyryl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-bromo-3-(4-methylstyryl)benzene(226712-71-6)
    11. EPA Substance Registry System: (E)-1-bromo-3-(4-methylstyryl)benzene(226712-71-6)
  • 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: 226712-71-6(Hazardous Substances Data)

226712-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226712-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,7,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 226712-71:
(8*2)+(7*2)+(6*6)+(5*7)+(4*1)+(3*2)+(2*7)+(1*1)=126
126 % 10 = 6
So 226712-71-6 is a valid CAS Registry Number.

226712-71-6Downstream Products

226712-71-6Relevant articles and documents

Method of photo-induced catalytic selective synthesis of Z- and E-olefins

-

Paragraph 0043, (2019/10/01)

The invention discloses a method of photo-induced catalytic selective synthesis of Z- and E-olefins. According to the method, a disubstituted acetylene compound is used as a starting raw material, a cheap acid is used as a hydrogen source, a phosphine is

Photo-induced catalytic method for selectively synthesizing cis olefin and trans olefin by using alcohol as hydrogen source

-

Paragraph 0087-0090, (2019/10/04)

The invention discloses a photo-induced catalytic method for selectively synthesizing a cis olefin and a trans olefin by using alcohol as a hydrogen source. According to the method, a di-substituted acetylene compound is used as an initial raw material, t

Method for catalytic-selectively synthesizing Z- and E-alkene through alcohol supply hydrogen iridium controlled by ligand

-

Paragraph 0081-0084, (2019/01/23)

The invention discloses a method for catalytic-selectively synthesizing Z- and E-alkene through alcohol supply hydrogen iridium controlled by a ligand. The method comprises the following steps: usinga disubstituted acetylene compound as a starting raw mat

Ligand-controlled iridium-catalyzed semihydrogenation of alkynes with ethanol: highly stereoselective synthesis of E- and Z-alkenes

Yang., Jinfei,Wang, Chengniu,Sun, Yufeng,Man, Xuyan,Li, Jinxia,Sun, Fei

supporting information, p. 1903 - 1906 (2019/05/02)

A ligand-controlled iridium-catalyzed semihydrogenation of alkynes to E- and Z-alkenes with ethanol was developed. Effective selectivity control was achieved by ligand regulation. The use of 1,2-bis(diphenylphosphino)ethane (DPPE) and 1,5-cyclooctadiene (COD) was critical for the stereoselective semihydrogenation of alkynes. The general applicability of this procedure was highlighted by the synthesis of more than 40 alkenes, with good stereoselectivities. The value of our approach in practical applications was investigated by studying the effects of pinosylvin and 4,4′-dihydroxystilbene (DHS) on zebrafish as a vertebrate model.

Synthesis of and ferromagnetic coupling in poly(phenylenevinylene)s bearing built-in t-butyl nitroxides

Nishide, Hiroyuki,Kaneko, Takashi,Toriu, Shuichi,Kuzumaki, Yoshihiro,Tsuchida, Eishun

, p. 499 - 508 (2007/10/03)

Poly[[2- or 4-[N-t-butyl-N-(triethylsiloxy- or t-butyldimethylsiloxy)amino]-1,4- or 1,2-phenylene]vinylene] was synthesized by polymerizing 4- or 2-bromo-2- or 4-[N-t-butyl-N-(triethylsiloxy- or t-butyldimethylsiloxy)amino]styrene with a palladium catalyst, respectively. They were deprotected and chemically oxidized to yield poly(1,4- or 1,2-phenylenevinylene)s bearing a 2- or 4-substituted built-in nitroxide radical. The polyradicals were chemically stable, and their spin concentration was increased to 0.8 spin/unit. A SQUID measurement which included the corresponding diradicals and triradicals indicated that a partial, but strong, intramolecular ferromagnetic coupling was established through the conjugated backbone, despite a spin defect in the side radical moiety, for the poly(1,2- phenylenevinylene) bearing 4-substituted built-in nitroxide radical.

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