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CAS

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1260770-82-8

4-(4-chlorophenyl)piperidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1260770-82-8 Structure

  • Basic information

    1. Product Name: 4-(4-chlorophenyl)piperidin-2-one
    2. Synonyms: 4-(4-chlorophenyl)piperidin-2-one
    3. CAS NO:1260770-82-8
    4. Molecular Formula: C11H12ClNO
    5. Molecular Weight: 209.67208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1260770-82-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 399.9±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1 +-.0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 16.16±0.40(Predicted)
    10. CAS DataBase Reference: 4-(4-chlorophenyl)piperidin-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(4-chlorophenyl)piperidin-2-one(1260770-82-8)
    12. EPA Substance Registry System: 4-(4-chlorophenyl)piperidin-2-one(1260770-82-8)

  • 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: 1260770-82-8(Hazardous Substances Data)

1260770-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1260770-82-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,7,7 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1260770-82:
(9*1)+(8*2)+(7*6)+(6*0)+(5*7)+(4*7)+(3*0)+(2*8)+(1*2)=148
148 % 10 = 8
So 1260770-82-8 is a valid CAS Registry Number.

1260770-82-8Downstream Products

1260770-82-8Relevant articles and documents

Rhodium-catalyzed asymmetric 1,4-addition of organoboron reagents to 5,6-dihydro-2(1H)-pyridinones. Asymmetric synthesis of 4-aryl-2-piperidinones

Senda,Ogasawara,Hayashi

, p. 6852 - 6856 (2007/10/03)

Catalytic asymmetric synthesis of 4-aryl-2-piperidinones was realized for the first time by asymmetric 1,4-addition of arylboron reagents to 5,6-dihydro-2(1H)-pyridinones in the presence of a chiral bisphosphine-rhodium catalyst. In the reaction introduci

Pyrrolidone and piperidone derivatives with antihistaminic and antianaphylactic activities. Synthesis and pharmacological study

de Meglio,Corradi,Ravenna,Gentili,Tempra-Gabbiati,Cristina,Riva

, p. 359 - 382 (2007/10/02)

The preparation of several derivatives to oxatomide (A), with the benzimidazolinone moiety replaced by another heterocyclic residue is described. In some cases changes to the basic chain of (A) were also considered. All the new compounds were evaluated as

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