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501127-42-0

2-Pyrimidinecarbonitrile, 5-bromo-4-(cyclohexylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501127-42-0 Structure

  • Basic information

    1. Product Name: 2-Pyrimidinecarbonitrile, 5-bromo-4-(cyclohexylamino)-
    2. Synonyms:
    3. CAS NO:501127-42-0
    4. Molecular Formula: C11H13BrN4
    5. Molecular Weight: 281.155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501127-42-0.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-Pyrimidinecarbonitrile, 5-bromo-4-(cyclohexylamino)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pyrimidinecarbonitrile, 5-bromo-4-(cyclohexylamino)-(501127-42-0)
    11. EPA Substance Registry System: 2-Pyrimidinecarbonitrile, 5-bromo-4-(cyclohexylamino)-(501127-42-0)

  • 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: 501127-42-0(Hazardous Substances Data)

501127-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501127-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,1,2 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501127-42:
(8*5)+(7*0)+(6*1)+(5*1)+(4*2)+(3*7)+(2*4)+(1*2)=90
90 % 10 = 0
So 501127-42-0 is a valid CAS Registry Number.

501127-42-0Downstream Products

501127-42-0Relevant articles and documents

Novel scaffold for cathepsin K inhibitors

Teno, Naoki,Miyake, Takahiro,Ehara, Takeru,Irie, Osamu,Sakaki, Junichi,Ohmori, Osamu,Gunji, Hiroki,Matsuura, Naoko,Masuya, Keiichi,Hitomi, Yuko,Nonomura, Kazuhiko,Horiuchi, Miyuki,Gohda, Keigo,Iwasaki, Atsuko,Umemura, Ichiro,Tada, Sachiyo,Kometani, Motohiko,Iwasaki, Genji,Cowan-Jacob, Sandra W.,Missbach, Martin,Lattmann, Rene,Betschart, Claudia

, p. 6096 - 6100 (2008/04/03)

Pyrrolopyrimidine, a novel scaffold, allows to adjust interactions within the S3 subsite of cathepsin K. The core intermediate 10 facilitated the P3 optimization and identified highly potent and selective cathepsin K inhibitors 11-20.

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