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CAS

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1313757-11-7

1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1313757-11-7 Structure

  • Basic information

    1. Product Name: 1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole
    2. Synonyms: 1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole
    3. CAS NO:1313757-11-7
    4. Molecular Formula:
    5. Molecular Weight: 362.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1313757-11-7.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: 1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole(1313757-11-7)
    11. EPA Substance Registry System: 1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole(1313757-11-7)

  • 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: 1313757-11-7(Hazardous Substances Data)

1313757-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313757-11-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,7,5 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1313757-11:
(9*1)+(8*3)+(7*1)+(6*3)+(5*7)+(4*5)+(3*7)+(2*1)+(1*1)=137
137 % 10 = 7
So 1313757-11-7 is a valid CAS Registry Number.

1313757-11-7Downstream Products

1313757-11-7Relevant articles and documents

Aluminum triflate as a powerful catalyst for direct amination of alcohols, including electron-withdrawing group-substituted benzhydrols

Ohshima, Takashi,Ipposhi, Junji,Nakahara, Yasuhito,Shibuya, Ryozo,Mashima, Kazushi

supporting information, p. 2447 - 2452 (2012/11/07)

Direct aminations of allylic alcohols, benzylic alcohols, and benzhydrols with electron-withdrawing (F, Br, I, NO2, or CN) substituents were efficiently catalyzed by aluminum triflate [Al(OTf)3] to afford the corresponding biarylamines in high yield, and the dibromo-substituted product was further transformed into letrozole. Copyright

Cobalt-catalyzed benzylic C-H amination via dehydrogenative-coupling reaction

Ye, Yang-Hong,Zhang, Ji,Wang, Gao,Chen, Shan-Yong,Yu, Xiao-Qi

supporting information; experimental part, p. 4649 - 4654 (2011/06/27)

An efficient direct benzylic C-H amination via dehydrogenative-coupling by using an inexpensive catalyst/oxidant (CoBr2/tBuOO tBu) system is described. Various unmodified amides including primary or secondary sulfonamides, carboxamides, and carbamates preformed well with benzylic hydrocarbons with moderate to good yields.

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