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CAS

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1191241-09-4

dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1191241-09-4 Structure

  • Basic information

    1. Product Name: dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate
    2. Synonyms: dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate
    3. CAS NO:1191241-09-4
    4. Molecular Formula:
    5. Molecular Weight: 368.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191241-09-4.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: dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate(1191241-09-4)
    11. EPA Substance Registry System: dimethyl 2-(4-oxo-4-phenyl-2-(p-tolyl)butyl)malonate(1191241-09-4)

  • 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: 1191241-09-4(Hazardous Substances Data)

1191241-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191241-09-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,2,4 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1191241-09:
(9*1)+(8*1)+(7*9)+(6*1)+(5*2)+(4*4)+(3*1)+(2*0)+(1*9)=124
124 % 10 = 4
So 1191241-09-4 is a valid CAS Registry Number.

1191241-09-4Downstream Products

1191241-09-4Relevant articles and documents

Ring Opening of Donor-Acceptor Cyclopropanes with Acyclic 1,3-Diketones for the Synthesis of 1,6-Dicarbonyl Compounds

Zhang, Dongxin,Cai, Hu,Chen, Yan,Yin, Lei,Zhong, Junchao,Zhang, Ying,Zhang, Qian-Feng

, p. 14262 - 14270 (2020)

1,6-Dicarbonyl compounds, representing the formal addition products of the α-position of acetophenone derivatives to donor-acceptor cyclopropanes, were synthesized in two steps via first ring opening of donor-acceptor cyclopropanes with acyclic 1,3-diketo

Switchable reactions of cyclopropanes with enol silyl ethers. Controllable synthesis of cyclopentanes and 1,6-dicarbonyl compounds

Qu, Jian-Ping,Deng, Chao,Zhou, Jian,Sun, Xiu-Li,Tang, Yong

scheme or table, p. 7684 - 7689 (2009/12/25)

(Chemical Equation Presented) Cu(SbF6)2-catalyzed reaction of 2-substituted cyclopropane-1,1-dicarboxylates 1 with enol silyl ethers 2 can be readily controlled: the reaction undergoes a cycloaddition to provide substituted cyclopent

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