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1502749-01-0

C22H17BrO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1502749-01-0 Structure

  • Basic information

    1. Product Name: C22H17BrO4
    2. Synonyms: C22H17BrO4
    3. CAS NO:1502749-01-0
    4. Molecular Formula:
    5. Molecular Weight: 425.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1502749-01-0.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: C22H17BrO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H17BrO4(1502749-01-0)
    11. EPA Substance Registry System: C22H17BrO4(1502749-01-0)

  • 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: 1502749-01-0(Hazardous Substances Data)

1502749-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1502749-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,0,2,7,4 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1502749-01:
(9*1)+(8*5)+(7*0)+(6*2)+(5*7)+(4*4)+(3*9)+(2*0)+(1*1)=140
140 % 10 = 0
So 1502749-01-0 is a valid CAS Registry Number.

1502749-01-0Upstream product

1502749-01-0Downstream Products

1502749-01-0Relevant articles and documents

Asymmetric diels-alder reaction of 3-olefinic benzofuran-2-ones and polyenals: Construction of chiral spirocyclic benzofuran-2-ones

Li, Xin,Lin, Mao-Hui,Han, Yu,Wang, Feng,Cheng, Jin-Pei

, p. 114 - 117 (2014)

A highly enantioselective Diels-Alder reaction of 3-olefinic benzofuran-2-ones with polyenals catalyzed by diphenylprolinolsilyl ether through a trienamine activation strategy was developed.

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