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CAS

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1370049-48-1

methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1370049-48-1 Structure

  • Basic information

    1. Product Name: methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate
    2. Synonyms: methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate
    3. CAS NO:1370049-48-1
    4. Molecular Formula:
    5. Molecular Weight: 252.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1370049-48-1.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: methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate(1370049-48-1)
    11. EPA Substance Registry System: methyl (E)-2-(2-phenylprop-1-en-1-yl)benzoate(1370049-48-1)

  • 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: 1370049-48-1(Hazardous Substances Data)

1370049-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1370049-48-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,0,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1370049-48:
(9*1)+(8*3)+(7*7)+(6*0)+(5*0)+(4*4)+(3*9)+(2*4)+(1*8)=141
141 % 10 = 1
So 1370049-48-1 is a valid CAS Registry Number.

1370049-48-1Downstream Products

1370049-48-1Relevant articles and documents

Selenium-mediated synthesis of tetrasubstituted naphthalenes through rearrangement

Tancock, James,Wirth, Thomas

, p. 10866 - 10872 (2015)

New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement pr

Stereoselective synthesis of hydroxy stilbenoids and styrenes by atom-efficient olefination with thiophthalides

Mitra, Prithiba,Shome, Brateen,Ranjan De, Saroj,Sarkar, Anindya,Mal, Dipakranjan

, p. 2742 - 2752 (2012/11/07)

The synthesis of stilbenoids and styryl carboxylic acids is accomplished with high E-stereoselectivity by olefination of aldehydes with thiophthalides under basic conditions. The olefination is highly atom-efficient as it only loses elemental sulfur during the reaction. This olefination, in conjunction with retro Kolbe-Schmitt reaction, allows facile synthesis of E-hydroxystilbenoids with minimal employment of protecting groups. This study also discloses two important findings: formation of i) 4-methylsulfanyl isocoumarins and ii) an 2-arylindenone. The Royal Society of Chemistry 2012.

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