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1072836-59-9

C23H23ClO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1072836-59-9 Structure

  • Basic information

    1. Product Name: C23H23ClO2
    2. Synonyms:
    3. CAS NO:1072836-59-9
    4. Molecular Formula:
    5. Molecular Weight: 366.887
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1072836-59-9.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: C23H23ClO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H23ClO2(1072836-59-9)
    11. EPA Substance Registry System: C23H23ClO2(1072836-59-9)

  • 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: 1072836-59-9(Hazardous Substances Data)

1072836-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072836-59-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,8,3 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072836-59:
(9*1)+(8*0)+(7*7)+(6*2)+(5*8)+(4*3)+(3*6)+(2*5)+(1*9)=159
159 % 10 = 9
So 1072836-59-9 is a valid CAS Registry Number.

1072836-59-9Downstream Products

1072836-59-9Relevant articles and documents

Indium-mediated alkynylation of Baylis-Hillman acetates: a novel route to 1,4-enynes

Yadav, Jhillu S.,Subba Reddy, Basi V.,Yadav, Nagendra Nath,Singh, Ashutosh Pratap,Choudhary, Madavi,Kunwar, Ajit C.

scheme or table, p. 6090 - 6094 (2009/04/04)

Baylis-Hillman acetates undergo smooth alkynylation with aryl-susbstituted iodoalkynes in the presence of indium metal in refluxing dichloromethane to furnish 1,4-enynes in high yields with (E)-stereoselectivity. In the absence of Lewis acid, the reaction follows both SN2 and SN2′ pathways affording 1:1 mixtures of 1,4-enynes. Upon addition of 10 mol % of InBr3, the reaction proceeds preferably in the SN2′ manner. In the case of adducts derived from acrylonitrile, the corresponding products are obtained in fairly good yields and with (Z)-stereoselectivity.

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