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CAS

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1308310-83-9

C13(11)CH11N3O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1308310-83-9 Structure

  • Basic information

    1. Product Name: C13(11)CH11N3O3
    2. Synonyms:
    3. CAS NO:1308310-83-9
    4. Molecular Formula:
    5. Molecular Weight: 268.249
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1308310-83-9.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: C13(11)CH11N3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13(11)CH11N3O3(1308310-83-9)
    11. EPA Substance Registry System: C13(11)CH11N3O3(1308310-83-9)

  • 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: 1308310-83-9(Hazardous Substances Data)

1308310-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1308310-83-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,8,3,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1308310-83:
(9*1)+(8*3)+(7*0)+(6*8)+(5*3)+(4*1)+(3*0)+(2*8)+(1*3)=119
119 % 10 = 9
So 1308310-83-9 is a valid CAS Registry Number.

1308310-83-9Downstream Products

1308310-83-9Relevant articles and documents

Sorafenib: Radiosynthesis and preliminary PET study of brain uptake in P-gp/Bcrp knockout mice

Asakawa, Chiharu,Ogawa, Masanao,Kumata, Katsushi,Fujinaga, Masayuki,Kato, Koichi,Yamasaki, Tomoteru,Yui, Joji,Kawamura, Kazunori,Hatori, Akiko,Fukumura, Toshimitsu,Zhang, Ming-Rong

, p. 2220 - 2223 (2011)

Sorafenib (Nexavar, BAY43-9006, 1) is a second-generation, orally active multikinase inhibitor that is approved for the treatment of some cancers in patients. In this Letter, we developed [11C]1 as a novel positron emission tomography (PET) probe, and evaluated the influence of ABC transporters-mediated efflux on brain uptake using PET with [11C]1 in P-glycoprotein (P-gp)/breast cancer resistance protein (Bcrp) knockout mice versus wild-type mice. [11C]1 was synthesized by the reaction of hydrochloride of aniline 2 with [11C]phosgene ([11C] COCl2) to give isocyanate [11C]6, followed by reaction with another aniline 3. Small-animal PET study with [11C]1 indicated that the radioactivity level (AUC0-60 min, SUV × min) in the brains of P-gp/Bcrp knockout mice was about three times higher than in wild-type mice.

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