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1094348-31-8

3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1094348-31-8 Structure

  • Basic information

    1. Product Name: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one
    2. Synonyms: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one
    3. CAS NO:1094348-31-8
    4. Molecular Formula:
    5. Molecular Weight: 246.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1094348-31-8.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-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(1094348-31-8)
    11. EPA Substance Registry System: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(1094348-31-8)

  • 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: 1094348-31-8(Hazardous Substances Data)

1094348-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1094348-31-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,3,4 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1094348-31:
(9*1)+(8*0)+(7*9)+(6*4)+(5*3)+(4*4)+(3*8)+(2*3)+(1*1)=158
158 % 10 = 8
So 1094348-31-8 is a valid CAS Registry Number.

1094348-31-8Relevant articles and documents

Fabrication of Pd/CuFe2O4 hybrid nanowires: A heterogeneous catalyst for Heck couplings

Lakshminarayana,Mahendar,Ghosal,Sreedhar,Satyanarayana,Subrahmanyam, Ch.

supporting information, p. 1646 - 1654 (2018/02/09)

The development of environmentally benign transformations is indispensable in organic synthesis. Herein, a hybrid heterogeneous catalyst, palladium(0) on copper ferrite nanowires, has been synthesized, characterized, and for the first time, employed in the Jeffrey Heck reaction between iodoarenes and allylic alcohols, and good to excellent yields have been obtained. In addition, the catalyst was found to be suitable for the usual Heck coupling. The nanocatalyst was recovered and reused up-to multiple runs without any noticeable loss of its catalytic activity.

Transition metal free chemoselective reduction of α,β-unsaturated ketones to saturated ketones using tosyl hydrazide as a hydrogen donor

Girish, Yarabally R.,Raghavendra, Kanchipura R.,Nagaraja, Dasappa,Kumar, Kothanahally S. Sharath,Shashikanth, Sheena

, p. 181 - 184 (2015/03/04)

An efficient, inexpensive and simple method for the reduction of various α,β-unsaturated ketones to corresponding saturated ketones using tosyl hydrazide as a hydrogen donor in DMF using calcium oxide powder has been reported. A variety of enones underwen

Rhodium(I)-catalyzed arylation of β-chloro ketones and related derivatives through domino dehydrochlorination/conjugate addition

Jiang, Quanbin,Guo, Tenglong,Wang, Qingfu,Wu, Ping,Yu, Zhengkun

supporting information, p. 1874 - 1880 (2013/07/19)

Highly efficient arylations of β-chloro ketones and their ester and amide derivatives were achieved by means of domino dehydrochlorination/Rh(I)- catalyzed conjugate addition. In situ generated vinyl ketones and their analogues were identified as the reaction intermediates. The present synthetic protocol provides a concise route to (chiral) β-aryl ketones, esters, and amides. Copyright

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