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5-benzyloxy-6-methoxynaphtho[1,2-b]furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 848780-31-4 Structure
  • Basic information

    1. Product Name: 5-benzyloxy-6-methoxynaphtho[1,2-b]furan
    2. Synonyms: 5-benzyloxy-6-methoxynaphtho[1,2-b]furan
    3. CAS NO:848780-31-4
    4. Molecular Formula:
    5. Molecular Weight: 320.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 848780-31-4.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: 5-benzyloxy-6-methoxynaphtho[1,2-b]furan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-benzyloxy-6-methoxynaphtho[1,2-b]furan(848780-31-4)
    11. EPA Substance Registry System: 5-benzyloxy-6-methoxynaphtho[1,2-b]furan(848780-31-4)
  • 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: 848780-31-4(Hazardous Substances Data)

848780-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848780-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,7,8 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 848780-31:
(8*8)+(7*4)+(6*8)+(5*7)+(4*8)+(3*0)+(2*3)+(1*1)=214
214 % 10 = 4
So 848780-31-4 is a valid CAS Registry Number.

848780-31-4Downstream Products

848780-31-4Relevant articles and documents

Synthesis and biological evaluation of (±)-cryptotanshinone and its simplified analogues as potent CDC25 inhibitors

Huang, Wei Gang,Jiang, Ying Yan,Li, Qian,Li, Jia,Li, Jing Ya,Lu, Wei,Cai, Jun Chao

, p. 1863 - 1870 (2005)

(±)-Cryptotanshinone and its simplified analogues were synthesized via SmI2 promoted radical cyclization to construct the furan ring. Analogues 18 and 26 were identified as effective inhibitors of dual specificity protein phosphatase CDC25B which is a key enzyme for cell cycle progression, and they also inhibited growth in A-549 human lung cancer cell line.

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