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174311-81-0

4-<(triphenylmethoxy)methyl>benzyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 174311-81-0 Structure

  • Basic information

    1. Product Name: 4-<(triphenylmethoxy)methyl>benzyl chloride
    2. Synonyms: 4-<(triphenylmethoxy)methyl>benzyl chloride
    3. CAS NO:174311-81-0
    4. Molecular Formula:
    5. Molecular Weight: 398.932
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 174311-81-0.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: 4-<(triphenylmethoxy)methyl>benzyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-<(triphenylmethoxy)methyl>benzyl chloride(174311-81-0)
    11. EPA Substance Registry System: 4-<(triphenylmethoxy)methyl>benzyl chloride(174311-81-0)

  • 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: 174311-81-0(Hazardous Substances Data)

174311-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174311-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,3,1 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174311-81:
(8*1)+(7*7)+(6*4)+(5*3)+(4*1)+(3*1)+(2*8)+(1*1)=120
120 % 10 = 0
So 174311-81-0 is a valid CAS Registry Number.

174311-81-0Relevant articles and documents

Mild and adaptable silver triflate-assisted method for trityl protection of alcohols in solution with solid-phase loading applications

Lundquist IV, Joseph T.,Satterfield, Andrew D.,Pelletier, Jeffrey C.

, p. 3915 - 3918 (2007/10/03)

Trityl ethers were prepared in solution in a matter of minutes by treating trityl chloride with silver triflate in the presence of alcohols. Yields were comparable or better than known literature methods. The method was compatible with the base-labile Fmo

Method for preparing alkylating agents and their use for alkylating cyclic ureas

-

, (2008/06/13)

This invention relates to methods for preparing alkylating agents and use of the agents prepared. In particular, this invention relates to preparation methods for hydroxy halide and organooxy halide alkylating agents and their use for alkylating cyclic urea compounds.

Stereoselective synthesis of HIV-1 protease inhibitor, DMP 323

Pierce,Pierce, Michael E.,Harris,Harris, Gregory D.,Islam,Islam, Qamrul,Radesca,Radesca, Lilian A.,Storace,Storace, Louis,Waltermire,Waltermire, Robert E.,Wat,Wat, Ed,Jadhav,Jadhav, Prabhakar K.,Emmett,Emmett, George C.

, p. 444 - 450 (2007/10/02)

DMP 323, a potent HIV-1 protease inhibitor, has been synthesized by an efficient stereoselective process, amenable to large scale preparations. The core C2 symmetric diol was synthesized by a stereoselective pinacol coupling of CBZ protected D-phenylalanine. Judicious selection of protecting groups allowed cyclic urea formation under mild conditions, enhanced the ease of bis-alkylation, and led te intermediates which were easily purified without chromatography. Additionally, a one-pot, high yield process was developed te prepare the alkylating agent, 4-[(triphenylmethoxy)methyl]benzyl chloride from 1,4-benzenedimethanol.

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