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2-Piperidinone, 1-(2-azido-5-chlorobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 797751-39-4 Structure
  • Basic information

    1. Product Name: 2-Piperidinone, 1-(2-azido-5-chlorobenzoyl)-
    2. Synonyms:
    3. CAS NO:797751-39-4
    4. Molecular Formula: C12H11ClN4O2
    5. Molecular Weight: 278.698
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 797751-39-4.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: 2-Piperidinone, 1-(2-azido-5-chlorobenzoyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Piperidinone, 1-(2-azido-5-chlorobenzoyl)-(797751-39-4)
    11. EPA Substance Registry System: 2-Piperidinone, 1-(2-azido-5-chlorobenzoyl)-(797751-39-4)
  • 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: 797751-39-4(Hazardous Substances Data)

797751-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 797751-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,7,7,5 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 797751-39:
(8*7)+(7*9)+(6*7)+(5*7)+(4*5)+(3*1)+(2*3)+(1*9)=234
234 % 10 = 4
So 797751-39-4 is a valid CAS Registry Number.

797751-39-4Downstream Products

797751-39-4Relevant articles and documents

A polymer-assisted solution-phase strategy for the synthesis of fused [2,1-b]quinazolinones and the preparation of optically active vasicinone

Kamal, Ahmed,Devaiah,Shankaraiah,Laxma Reddy

, p. 2609 - 2612 (2008/09/16)

An efficient preparation of fused [2,1-b]quinazolinones has been developed utilizing polymer-supported reagents. (±)- Vasicinone was converted into its dione by oxidation with poly (4-vinylpyridiniumdichromate). An efficient method has been developed for the synthesis of (d)- and (l)-vasicinone via asymmetric reduction of pyrrolo[2,1-b]quinazoline-3,9-dione by employing NaBH4/Me3SiCl as the reducing agent and polymer-supported chiral sulfonamide as catalyst. Georg Thieme Verlag Stuttgart.

One pot conversion of azido arenes to N-arylacetamides and N-arylformamides: Synthesis of 1,4-benzodiazepine-2,5-diones and fused [2,1-b]quinazolinones

Kamal, Ahmed,Ramana, A. Venkata,Reddy, K. Srinivasa,Ramana, K. Venkata,Hari Babu,Prasad, B. Rajendra

, p. 8187 - 8190 (2007/10/03)

Sodium iodide in acidic media has been employed for the synthesis of N-arylformamides and N-arylacetamides. The NaI/acetic acid reagent system has also been extended for the synthesis of 1,4-benzodiazepine-2,5-diones, pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones, and fused [2,1-b]quinazolinones.

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