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CAS

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1514927-05-9

1-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1514927-05-9 Structure

  • Basic information

    1. Product Name: 1-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone
    2. Synonyms: 1-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone
    3. CAS NO:1514927-05-9
    4. Molecular Formula:
    5. Molecular Weight: 353.218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1514927-05-9.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-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone(1514927-05-9)
    11. EPA Substance Registry System: 1-(8-quinolinyl)-4-(3-bromophenyl)-azetidinone(1514927-05-9)

  • 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: 1514927-05-9(Hazardous Substances Data)

1514927-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1514927-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,1,4,9,2 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1514927-05:
(9*1)+(8*5)+(7*1)+(6*4)+(5*9)+(4*2)+(3*7)+(2*0)+(1*5)=159
159 % 10 = 9
So 1514927-05-9 is a valid CAS Registry Number.

1514927-05-9Downstream Products

1514927-05-9Relevant articles and documents

Stereoselective synthesis of diazabicyclic β-lactams through intramolecular amination of unactivated C(sp3)-H bonds of carboxamides by palladium catalysis

Zhang, Shi-Jin,Sun, Wen-Wu,Cao, Pei,Dong, Xiao-Ping,Liu, Ji-Kai,Wu, Bin

, p. 956 - 968 (2016)

An efficient C(sp3)-H bond activation and intramolecular amination reaction via palladium catalysis at the β-position of carboxyamides to make β-lactams was described. The investigation of the substrate scope showed that the current reaction conditions favored activation of the β-methylene group. Short sequences were developed for preparation of various diazabicyclic β-lactam compounds with this method as the key step from chiral proline and piperidine derivatives.

N-quinolyl-substituted β-lactam compound and its pharmaceutical compositions and synthetic method and application

-

Paragraph 0120-0123, (2016/10/09)

The invention discloses an N-quinolyl substituted beta-lactam compound as shown in a general formula (I), wherein R and R refer to mutually independent H or C1-12 straight-chain or branched-chain hydrocarbonyl, aryl, alkoxy, acyloxy or amino; R r

Palladium-catalyzed unactivated c(sp3)-h bond activation and intramolecular amination of carboxamides: A new approach to β-lactams

Sun, Wen-Wu,Cao, Pei,Mei, Ren-Qiang,Li, Yue,Ma, Yuan-Liang,Wu, Bin

supporting information, p. 480 - 483 (2014/04/03)

An efficient method to synthesize the β-lactams with high regioselectivity via Pd-catalyzed C(sp3)-H bond activation and intramolecular amination of simple and readily available aminoquinoline carboxamides was demonstrated. C6F5I plays a signif

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