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4-(3-bromo-4-methylbenzoyl)morpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 443637-62-5 Structure
  • Basic information

    1. Product Name: 4-(3-bromo-4-methylbenzoyl)morpholine
    2. Synonyms: 4-(3-bromo-4-methylbenzoyl)morpholine;(3-bromo-4-methylphenyl)(morpholin-4-yl)methanone
    3. CAS NO:443637-62-5
    4. Molecular Formula: C12H14BrNO2
    5. Molecular Weight: 284.14906
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 443637-62-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(3-bromo-4-methylbenzoyl)morpholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-bromo-4-methylbenzoyl)morpholine(443637-62-5)
    11. EPA Substance Registry System: 4-(3-bromo-4-methylbenzoyl)morpholine(443637-62-5)
  • 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: 443637-62-5(Hazardous Substances Data)

443637-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443637-62-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,6,3 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 443637-62:
(8*4)+(7*4)+(6*3)+(5*6)+(4*3)+(3*7)+(2*6)+(1*2)=155
155 % 10 = 5
So 443637-62-5 is a valid CAS Registry Number.

443637-62-5Relevant articles and documents

PYRROLOPYRIMIDIN DERIVATIVE FOR USE AS PI3K INHIBITOR, AND USE THEREOF

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Page/Page column 34, (2010/11/03)

A preventive or therapeutic agent of a proliferative disease such as cancer, having superior PI3K inhibitory effects, superior cell proliferation inhibitory action as well as superior stability in a body and water solubility, is provided. A compound represented by formula (I): [wherein, Q represents a linking group represented by -X-Y-; X represents a single bond -CO-, -CONH-, -CON(C1-4 alkyl)-, -CS-, -CSNH-, -CSN(C1-4 alkyl)-, or -SO2-; Y represents a single bond, arylene or heteroarylene; provided that X and Y are not simultaneously single bonds; and R1 represents -C0-6 alkylene-(A)m-C1-6 alkyl, or C0-6 alkylene-(A)m-C0-6 alkylene-(heterocycle)] or a pharmaceutically acceptable salt thereof.

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