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1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1264739-88-9 Structure
  • Basic information

    1. Product Name: 1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one
    2. Synonyms: 1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one
    3. CAS NO:1264739-88-9
    4. Molecular Formula:
    5. Molecular Weight: 326.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1264739-88-9.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: 1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one(1264739-88-9)
    11. EPA Substance Registry System: 1-benzyl-3,4-dichloro-3-ethylhexahydro-1H-indol-2(3H)-one(1264739-88-9)
  • 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: 1264739-88-9(Hazardous Substances Data)

1264739-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264739-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,7,3 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1264739-88:
(9*1)+(8*2)+(7*6)+(6*4)+(5*7)+(4*3)+(3*9)+(2*8)+(1*8)=189
189 % 10 = 9
So 1264739-88-9 is a valid CAS Registry Number.

1264739-88-9Upstream product

1264739-88-9Relevant articles and documents

A green way to γ-lactams through a copper catalyzed ARGET-ATRC in ethanol and in the presence of ascorbic acid

Casolari, Roberto,Felluga, Fulvia,Frenna, Vincenzo,Ghelfi, Franco,Pagnoni, Ugo M.,Parsons, Andrew F.,Spinelli, Domenico

, p. 408 - 416 (2011)

A 'green' ARGET-ATRC, for the CuCl[PMDETA] catalysed cyclo-isomerization of N-allyl-α-polychloroamides to γ-lactams is described. The process works efficiently (yields 78-96%), uses a bio-solvent, as ethanol, and exploits the reducing feature of ascorbic acid to limit, at a low level (2-4%), the amount of catalyst. To preserve the efficacy of the catalytic cycle, addition of Na2CO3 is essential, which quenches the HCl released during the CuCl[PMDETA] regeneration step. Profitable features of the process are: mild reaction temperatures (25-37 °C), relatively short reaction times (usually 5 h) and low solvent volumes (2 mmol of substrate/mL of ethanol). The method, upon stoichiometric adjustment, was also used for the synthesis of α,β-unsaturated-γ-lactams from N-(2-chloroallyl)-α- polychloroamides, via a tandem process involving an ATRC and a reductive [1,2]-elimination. Copyright

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