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  • 1427310-66-4 Structure
  • Basic information

    1. Product Name: C29H36FN7O2
    2. Synonyms: C29H36FN7O2
    3. CAS NO:1427310-66-4
    4. Molecular Formula:
    5. Molecular Weight: 533.649
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427310-66-4.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: C29H36FN7O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H36FN7O2(1427310-66-4)
    11. EPA Substance Registry System: C29H36FN7O2(1427310-66-4)
  • 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: 1427310-66-4(Hazardous Substances Data)

1427310-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427310-66-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,3,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1427310-66:
(9*1)+(8*4)+(7*2)+(6*7)+(5*3)+(4*1)+(3*0)+(2*6)+(1*6)=134
134 % 10 = 4
So 1427310-66-4 is a valid CAS Registry Number.

1427310-66-4Relevant articles and documents

Amino acid derived quinazolines as Rock/PKA inhibitors

Chowdhury, Sarwat,Chen, Yen Ting,Fang, Xingang,Grant, Wayne,Pocas, Jennifer,Cameron, Michael D.,Ruiz, Claudia,Lin, Li,Park, Hajeung,Schr?ter, Thomas,Bannister, Thomas D.,Lograsso, Philip V.,Feng, Yangbo

, p. 1592 - 1599 (2013/04/10)

SAR and lead optimization studies for Rock inhibitors based on amino acid-derived quinazolines are described. Studies demonstrated that these amino acid derived quinazolinones were mainly pan-Rock (I & II) inhibitors. While selectivity against other kinas

QUINAZOLINE DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 104, (2010/06/15)

The invention is directed to quinazoline compounds that can inhibit the bioactivity of one or more kinase enzymes, including a Rho kinase, an AKT kinase, a p70S6K kinase, a LIM kinase, an IKK kinase, a Fit kinase, an Aurora kinase, or a Src kinase, or any combination thereof; to methods of use of those compounds; and to methods of preparation of those compounds. The inventive compounds can be used in the treatment of malconditions including cardiovascular disease, neurogenic pain, hypertension, atherosclerosis, angina, stroke, arterial obstruction, peripheral arterial disease, erectile dysfunction, acute and chronic pain, dementia, Alzheimer's disease, Parkinson's disease, neuronal degeneration, asthma, amyotrophic lateral sclerosis, spinal cord injury, rheumatoid arthritis, osteoarthritis, osteoporosis, psoriasis, cerebral vasospasm, open angle glaucoma, multiple sclerosis, pulmonary hypertension, acute respiratory distress syndrome, inflammation, diabetes, urinary organ diseases and benign prostatic hypertrophy (BPH), metastasis, cancer, glaucoma, ocular hypertension, retinopathy, autoimmune disease, viral infection, or myocardial pathology.

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