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59184-12-2

4-mesityl-3,5-dimethylisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 59184-12-2 Structure

  • Basic information

    1. Product Name: 4-mesityl-3,5-dimethylisoxazole
    2. Synonyms: 4-mesityl-3,5-dimethylisoxazole
    3. CAS NO:59184-12-2
    4. Molecular Formula:
    5. Molecular Weight: 215.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59184-12-2.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: 4-mesityl-3,5-dimethylisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-mesityl-3,5-dimethylisoxazole(59184-12-2)
    11. EPA Substance Registry System: 4-mesityl-3,5-dimethylisoxazole(59184-12-2)

  • 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: 59184-12-2(Hazardous Substances Data)

59184-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59184-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,8 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59184-12:
(7*5)+(6*9)+(5*1)+(4*8)+(3*4)+(2*1)+(1*2)=142
142 % 10 = 2
So 59184-12-2 is a valid CAS Registry Number.

59184-12-2Downstream Products

59184-12-2Relevant articles and documents

[PdA (IPr*) (cinnamyl)Cl]: An efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling

Chartoire, Anthony,Lesieur, Mathieu,Falivene, Laura,Slawin, Alexandra M. Z.,Cavallo, Luigi,Cazin, Catherine S. J.,Nolan, Steven P.

supporting information; experimental part, p. 4517 - 4521 (2012/05/04)

The bigger the better: The new well-defined [Pd(IPr*)(cin)Cl] pre-catalyst is described (see scheme). This complex proves to be highly active in the Suzuki-Miyaura cross-coupling for the synthesis of tetra-ortho- substituted biaryls under mild conditions.

A general and special catalyst for suzuki-miyaura coupling processes

Tang, Wenjun,Capacci, Andrew G.,Wei, Xudong,Li, Wenjie,White, Andre,Patel, Nitinchandra D.,Savoie, Jolaine,Gao, Joe J.,Rodriguez, Sonia,Qu, Bo,Haddad, Nizar,Lu, Bruce Z.,Krishnamurthy, Dhileepkumar,Yee, Nathan K.,Senanayake, Chris H.

supporting information; experimental part, p. 5879 - 5883 (2010/10/01)

(Figure Presented) Biaryl monophosphorus ligands containing a 2,3-dihydrobenzo[d][1,3]oxaphosphole framework are highly effective for the palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of a wide range of substrates. Ligand 1 has demonstrated excellent performance for coupling reactions of extremely hindered arylboronic acids.

Pd-PEPPSI-IPent: Low-temperature negishi cross-coupling for the preparation of highly functionalized, tetra-ortho-substituted biaryls

Calimsiz, Selcuk,Sayah, Mahmoud,Mallik, Debasis,Organ, Michael G.

supporting information; experimental part, p. 2014 - 2017 (2010/06/20)

(Chemical Equation Presented) Cool couplings: Complex, hindered biaryls have been prepared at temperatures ranging from 0°C to room temperature, or with gentle heating. The Pd-PEPPSI-IPent catalyst (see scheme) nicely couples starting materials containing acidic moieties and routinely prepares biaryl derivatives where one or both rings comprising the biaryl are heterocyclic. Ar1=hindered aryl or heteroaryl, Ar2=unactivated aryl or heteroaryl.

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