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247043-57-8

Phosphonic acid, [2-(benzoylamino)-2-oxoethyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 247043-57-8 Structure

  • Basic information

    1. Product Name: Phosphonic acid, [2-(benzoylamino)-2-oxoethyl]-, diethyl ester
    2. Synonyms:
    3. CAS NO:247043-57-8
    4. Molecular Formula: C13H18NO5P
    5. Molecular Weight: 299.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247043-57-8.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: Phosphonic acid, [2-(benzoylamino)-2-oxoethyl]-, diethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonic acid, [2-(benzoylamino)-2-oxoethyl]-, diethyl ester(247043-57-8)
    11. EPA Substance Registry System: Phosphonic acid, [2-(benzoylamino)-2-oxoethyl]-, diethyl ester(247043-57-8)

  • 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: 247043-57-8(Hazardous Substances Data)

247043-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247043-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,0,4 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 247043-57:
(8*2)+(7*4)+(6*7)+(5*0)+(4*4)+(3*3)+(2*5)+(1*7)=128
128 % 10 = 8
So 247043-57-8 is a valid CAS Registry Number.

247043-57-8Relevant articles and documents

Inhibitory effects of N-(acryloyl)benzamide derivatives on tyrosinase and melanogenesis

Lee, Sanggwon,Ullah, Sultan,Park, Chaeun,Won Lee, Hee,Kang, Dongwan,Yang, Jungho,Akter,Park,Chun, Pusoon,Moon, Hyung Ryong

, p. 3929 - 3937 (2019)

Targeting of tyrosinase has proven to be the best means of identifying safe, efficacious, and potent tyrosinase inhibitors for whitening skin. We designed and synthesized ten NAB (N-(acryloyl)benzamide) derivatives (1a–1j) using the Horner-Wadsworth-Emmon

Catalytic Asymmetric Total Syntheses of Quinine and Quinidine

Raheem, Izzat T.,Goodman, Steven N.,Jacobsen, Eric N.

, p. 706 - 707 (2007/10/03)

The catalytic, asymmetric syntheses of quinine and quinidine were achieved in 16 steps. The recently developed salen(Al)-catalyzed enantioselective Michael addition of methyl cyanoacetate served to set the crucial C4 stereocenter in 92% ee, and a late-stage asymmetric dihydroxylation was used to differentiate the common intermediate and access the two desired diastereomeric products with high selectivity. Copyright

A Practical Synthesis of α,β-Unsaturated Imides, Useful Substrates for Asymmetric Conjugate Addition Reactions

Goodman, Steven N.,Jacobsen, Eric N.

, p. 953 - 956 (2007/10/03)

We report an improved synthesis of α,β-unsaturated imides, a class of compounds that has been identified as broadly useful in (salen)aluminum-catalyzed asymmetric conjugate addition reactions. An efficient, scaleable procedure for the synthesis of phospho

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