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CAS

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157430-07-4

(4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157430-07-4 Structure

  • Basic information

    1. Product Name: (4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanone
    2. Synonyms:
    3. CAS NO:157430-07-4
    4. Molecular Formula:
    5. Molecular Weight: 526.675
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157430-07-4.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: (4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanone(157430-07-4)
    11. EPA Substance Registry System: (4-Benzyloxy-3,5-dimethoxy-phenyl)-(2-[1,3]dithian-2-yl-4,5-dimethoxy-phenyl)-methanone(157430-07-4)

  • 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: 157430-07-4(Hazardous Substances Data)

157430-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157430-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,4,3 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 157430-07:
(8*1)+(7*5)+(6*7)+(5*4)+(4*3)+(3*0)+(2*0)+(1*7)=124
124 % 10 = 4
So 157430-07-4 is a valid CAS Registry Number.

157430-07-4Downstream Products

157430-07-4Relevant articles and documents

A Rapid Entry into Podophyllotoxin Congeners: Synthesis of Justicidin B

Kamal, Ahmed,Daneshtalab, Mohsen,Micetich, Ronald G.

, p. 3879 - 3882 (2007/10/02)

A facile synthesis of justicidin B is described, as well as related podophyllum lignans by employing Michael Initiated Ring Clousere Strategy followed by desulfurization mediated by nickel-containing complex reducing agent. - Key words: podophyllotoxin, podophyllum lignans, justicidin B., Michael initiated Ring Closure, desulfurization, nickel-containing complex reducing agent.

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