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methyl (4-formylbenzoyl)valinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 910056-11-0 Structure
  • Basic information

    1. Product Name: methyl (4-formylbenzoyl)valinate
    2. Synonyms: methyl (4-formylbenzoyl)valinate
    3. CAS NO:910056-11-0
    4. Molecular Formula:
    5. Molecular Weight: 263.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 910056-11-0.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 (4-formylbenzoyl)valinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (4-formylbenzoyl)valinate(910056-11-0)
    11. EPA Substance Registry System: methyl (4-formylbenzoyl)valinate(910056-11-0)
  • 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: 910056-11-0(Hazardous Substances Data)

910056-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910056-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,0,5 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 910056-11:
(8*9)+(7*1)+(6*0)+(5*0)+(4*5)+(3*6)+(2*1)+(1*1)=120
120 % 10 = 0
So 910056-11-0 is a valid CAS Registry Number.

910056-11-0Relevant articles and documents

Metal- And additive-free C-H oxygenation of alkylarenes by visible-light photoredox catalysis

García Manche?o, Olga,Kuhlmann, Jan H.,Pérez-Aguilar, María Carmen,Piekarski, Dariusz G.,Uygur, Mustafa

, p. 3392 - 3399 (2021)

A metal- and additive-free methodology for the highly selective, photocatalyzed C-H oxygenation of alkylarenes under air to the corresponding carbonyls is presented. The process is catalyzed by an imide-acridinium that forms an extremely strong photooxidant upon visible light irradiation, which is able to activate inert alkylarenes such as toluene. Hence, this is an easy to perform, sustainable and environmentally friendly oxidation that provides valuable carbonyls from abundant, readily available compounds.

A convenient [2+2] cycloaddition-cycloreversion reaction for the synthesis of 1,1-dicyanobuta-1,3-diene-scaffolded peptides as new imaging chromophores

Rijkers, Dirk T.S.,De Prada López, Fernando,Liskamp, Rob M.J.,Diederich, Franois

scheme or table, p. 6963 - 6967 (2012/02/13)

We report on the chemoselective coupling between colorless peptide fragments functionalized with a mutually reactive electron-rich N α-(4-ethynylphenyl)-Nα-(methyl)-glycyl- and an electron-deficient [4-(2,2-dicyanovinyl)]benzoyl moie

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