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135705-49-6

3-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135705-49-6 Structure

  • Basic information

    1. Product Name: 3-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester
    2. Synonyms: 3-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester
    3. CAS NO:135705-49-6
    4. Molecular Formula:
    5. Molecular Weight: 433.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135705-49-6.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-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester(135705-49-6)
    11. EPA Substance Registry System: 3-(2-Ethoxycarbonyl-1-phenyl-ethylselanyl)-3-phenyl-propionic acid ethyl ester(135705-49-6)

  • 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: 135705-49-6(Hazardous Substances Data)

135705-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135705-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,0 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135705-49:
(8*1)+(7*3)+(6*5)+(5*7)+(4*0)+(3*5)+(2*4)+(1*9)=126
126 % 10 = 6
So 135705-49-6 is a valid CAS Registry Number.

135705-49-6Upstream product

135705-49-6Downstream Products

135705-49-6Relevant articles and documents

Reactions of sodium hydrogen selenide with α,β-unsaturated compounds

Cartaya-Marin,Rissolo

, p. 951 - 957 (1991)

Sodium hydrogen selenide (NaHSe) reacts with α,β-unsaturated compounds, under mild conditions, via a Michael type of addition to yield the corresponding monoselenides.

Selective Reduction of α,β-Unsaturated Carbonyl Compounds with Carbon Monoxide and Water Assisted by Seleniium

Nishiyama, Yutaka,Makino, Yasuhiko,Hamanaka, Sawako,Ogawa, Akiya,Sonoda, Noboru

, p. 1682 - 1684 (2007/10/02)

Carbon-carbon double bond of α,β-unsaturated carbonyl compounds can be reduced selectively with hydrogen selenide, generated in situ by the reaction of elemental selenium with carbon monoxide and water in the presence of strongly basic tertiary amine.

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