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  • 916139-29-2 Structure
  • Basic information

    1. Product Name: C32H51NO5
    2. Synonyms: C32H51NO5
    3. CAS NO:916139-29-2
    4. Molecular Formula:
    5. Molecular Weight: 529.761
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 916139-29-2.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: C32H51NO5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H51NO5(916139-29-2)
    11. EPA Substance Registry System: C32H51NO5(916139-29-2)
  • 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: 916139-29-2(Hazardous Substances Data)

916139-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916139-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,1,3 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 916139-29:
(8*9)+(7*1)+(6*6)+(5*1)+(4*3)+(3*9)+(2*2)+(1*9)=172
172 % 10 = 2
So 916139-29-2 is a valid CAS Registry Number.

916139-29-2Upstream product

916139-29-2Downstream Products

916139-29-2Relevant articles and documents

Synthesis and antiproliferative evaluation of 23-hydroxybetulinic acid derivatives

Lan, Ping,Wang, Jiao,Zhang, Dong-Mei,Shu, Chang,Cao, Hui-Hui,Sun, Ping-Hua,Wu, Xiao-Ming,Ye, Wen-Cai,Chen, Wei-Min

, p. 2490 - 2502 (2011)

Based on structural modifications of the natural 23-hydroxybetulinic acid, a series of novel its derivatives had been synthesized. The new compounds were screened for in vitro antiproliferative activity against cancer cell lines HeLa, MCF-7, HepG2, B16 and A375 using doxorubicin as a reference. The vast majority of derivatives had exhibited potent tumor growth inhibitory activity than original compound. The derivatives 4, 5, 7, 20, 23, 26, 43 and 44 with IC 50 values lower than 10 μM on all tested cell lines were regarded as the most promising compounds. The structure-activity relationships of 23-hydroxybetulinic acid derivatives were also discussed in the present investigations.

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