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CAS

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250613-23-1

3-(p-tolyl)but-3-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 250613-23-1 Structure

  • Basic information

    1. Product Name: 3-(p-tolyl)but-3-en-2-one
    2. Synonyms: 3-(p-tolyl)but-3-en-2-one
    3. CAS NO:250613-23-1
    4. Molecular Formula:
    5. Molecular Weight: 160.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 250613-23-1.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: 3-(p-tolyl)but-3-en-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(p-tolyl)but-3-en-2-one(250613-23-1)
    11. EPA Substance Registry System: 3-(p-tolyl)but-3-en-2-one(250613-23-1)

  • 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: 250613-23-1(Hazardous Substances Data)

250613-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250613-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,6,1 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 250613-23:
(8*2)+(7*5)+(6*0)+(5*6)+(4*1)+(3*3)+(2*2)+(1*3)=101
101 % 10 = 1
So 250613-23-1 is a valid CAS Registry Number.

250613-23-1Upstream product

250613-23-1Downstream Products

250613-23-1Relevant articles and documents

Expedient Access to 2,3-Dihydropyridines from Unsaturated Oximes by Rh(III)-Catalyzed C-H Activation

Romanov-Michailidis, Fedor,Sedillo, Kassandra F.,Neely, Jamie M.,Rovis, Tomislav

, p. 8892 - 8895 (2015)

α,β-Unsaturated oxime pivalates are proposed to undergo reversible C(sp2)-H insertion with cationic Rh(III) complexes to furnish five-membered metallacycles. In the presence of 1,1-disubstituted olefins, these species participate in irreversible migratory insertion to give, after reductive elimination, 2,3-dihydropyridine products in good yields. Catalytic hydrogenation can then be used to convert these molecules into piperidines, which are important structural components of numerous pharmaceuticals.

Enantioselective synthesis of β-substituted chiral allylic amines: Via Rh-catalyzed asymmetric hydrogenation

Wang, Qingli,Gao, Wenchao,Lv, Hui,Zhang, Xumu

, p. 11850 - 11853 (2016/10/07)

An asymmetric mono-hydrogenation of 2-acetamido-1,3-dienes catalyzed by a Rh-DuanPhos complex has been developed. This approach provides easy access to chiral allylic amines with excellent enantioselectivities and high regioselectivities. The products are valuable chiral building blocks for pharmaceuticals.

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