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dibromo(o-tolyl)borane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156629-31-1 Structure
  • Basic information

    1. Product Name: dibromo(o-tolyl)borane
    2. Synonyms: dibromo(o-tolyl)borane
    3. CAS NO:156629-31-1
    4. Molecular Formula:
    5. Molecular Weight: 261.752
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156629-31-1.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: dibromo(o-tolyl)borane(CAS DataBase Reference)
    10. NIST Chemistry Reference: dibromo(o-tolyl)borane(156629-31-1)
    11. EPA Substance Registry System: dibromo(o-tolyl)borane(156629-31-1)
  • 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: 156629-31-1(Hazardous Substances Data)

156629-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156629-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,6,2 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156629-31:
(8*1)+(7*5)+(6*6)+(5*6)+(4*2)+(3*9)+(2*3)+(1*1)=151
151 % 10 = 1
So 156629-31-1 is a valid CAS Registry Number.

156629-31-1Relevant articles and documents

Asymmetric Total Synthesis of Lancifodilactone G Acetate

Liu, Dong-Dong,Sun, Tian-Wen,Wang, Kuang-Yu,Lu, Yong,Zhang, Su-Lei,Li, Yuan-He,Jiang, Yan-Long,Chen, Jia-Hua,Yang, Zhen

, p. 5732 - 5735 (2017)

Asymmetric total synthesis of structurally intriguing and highly oxygenated lancifodilactone G acetate (7) has been achieved for the first time in 28 steps from a cheap commodity chemical, 2-(triisopropylsiloxy)-1,3-butadiene.

Catalytic and Enantioselective Diels-Alder Reactions of (E)-4-Oxopent-2-enoates

Zhang, Su-Lei,Lu, Yong,Li, Yuan-He,Wang, Kuang-Yu,Chen, Jia-Hua,Yang, Zhen

, p. 3986 - 3989 (2017)

Novel oxazaborolidines activated by the strong acid triflimide or AlBr3 form cationic chiral catalysts. These are effective catalysts for highly regio- and enantioselective Diels-Alder reactions using substituted (E)-4-oxopent-2-enoates as dienophiles.

Cationic Chiral Fluorinated Oxazaborolidines. More Potent, Second-Generation Catalysts for Highly Enantioselective Cycloaddition Reactions

Mahender Reddy, Karla,Bhimireddy, Eswar,Thirupathi, Barla,Breitler, Simon,Yu, Shunming,Corey

supporting information, p. 2443 - 2453 (2016/03/08)

The coordination of chiral ligands to Lewis acid metal derivatives, a useful strategy for enantioselective, electrophilic catalysis, generally leads to a lower level of catalytic activity than that of the original uncomplexed compound. Activation by furth

Highly Enantioselective diels-alder reactions of maleimides catalyzed by activated chiral oxazaborolidines

Mukherjee, Santanu,Corey

experimental part, p. 632 - 635 (2010/06/17)

[Chemical equation presented] Diels-Alder reactions of various combinations of maleimides and 1,3-dienes with cationic oxazaborolidines as catalysts have been shown to be highly efficient and enantioselective.

Synthesis and characterization of triarylborthiins, Ar3B3S3 (Ar=4-MeC6H4, 3-MeC6H4, 2-MeC6H4, 4-EtC6H4, and 3,5-Me2C6H3)

Beckett, Michael A.,Minton, Paul R.,Werschkun, Barbara

, p. 37 - 42 (2007/10/02)

The air/moisture-sensitive triarylborthiins, Ar3B3S3 (Ar=4-MeC6H4, 3-MeC6H4, 2-MeC6H4, 4-EtC6H4, and 3,5-Me2C6H3), have been prepared by the reaction of ArBBr2 with HgS in benzene at reflux and have been characterized by 11B NMR and IR spectroscopy and ma

A New Borylation Method for Alkylbenzene and Polystyrene

Paetzold, Peter,Hoffmann, Juergen

, p. 3724 - 3733 (2007/10/02)

The borylation of alkylbenzenes by Hal2BH (Hal = F, Cl, Br) gives H2 and a mixture of m- and p-alkyl(dihaloboryl)benzenes.In the case of bulky alkyl groups, such as isopropyl, tert-butyl, these are partially split off as R - H and RBHal2.The phenyl groups in polystyrene-divinylbenzene copolymers undergo borylation with Br2BH in a 55percent yield.

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