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128133-75-5

benzyl-(3-bromophenyl)-sulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128133-75-5 Structure

  • Basic information

    1. Product Name: benzyl-(3-bromophenyl)-sulfide
    2. Synonyms: benzyl-(3-bromophenyl)-sulfide
    3. CAS NO:128133-75-5
    4. Molecular Formula:
    5. Molecular Weight: 279.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128133-75-5.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: benzyl-(3-bromophenyl)-sulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl-(3-bromophenyl)-sulfide(128133-75-5)
    11. EPA Substance Registry System: benzyl-(3-bromophenyl)-sulfide(128133-75-5)

  • 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: 128133-75-5(Hazardous Substances Data)

128133-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128133-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,3 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128133-75:
(8*1)+(7*2)+(6*8)+(5*1)+(4*3)+(3*3)+(2*7)+(1*5)=115
115 % 10 = 5
So 128133-75-5 is a valid CAS Registry Number.

128133-75-5Relevant articles and documents

Design of D-π-A type photoacid generators for high efficiency excitation at 405 nm and 800 nm

Jin, Ming,Xu, Haoran,Hong, Hong,Malval, Jean-Pierre,Zhang, Yuan,Ren, Aimin,Wan, Decheng,Pu, Hongting

supporting information, p. 8480 - 8482 (2013/09/23)

New sulfonium salts with diphenylamino asymmetrically substituted stilbene as a D-π-A conjugated system have been synthesized. The resulting photoacid generators exhibit a highly efficient acid photogeneration process by either one-photon 405 nm or two-ph

SULPHUR-LINKED COMPOUNDS FOR TREATING OPHTHALMIC DISEASES AND DISORDERS

-

Page/Page column 101, (2010/04/30)

Provided are sulphur-linked compounds, pharmaceutical compositions thereof, and methods of treating ophthalmic diseases and disorders, such as age-related macular degeneration and Stargardt's Disease, using said compounds and compositions.

Gold-catalyzed C-S bond formation from thiols

Jean, Micka?l,Renault, Jacques,van de Weghe, Pierre,Asao, Naoki

supporting information; experimental part, p. 378 - 381 (2010/03/24)

ortho-Alkynylbenzoic acid alkyl esters act as alkylating agents of thiol derivatives with PPh3AuCl in combination with AgOTf in 1,2-dichloroethane at 80 °C. The corresponding sulfide compounds are obtained in good to excellent yields.

Synthesis of aryl benzyl NH-sulfoximines

Barry, Nicola,Brondel, Nicolas,Lawrence, Simon E.,Maguire, Anita R.

experimental part, p. 10660 - 10670 (2010/01/16)

Efficient synthesis and characterisation of a series of aryl benzyl NH-sulfoximines are described. While N-protected versions of aryl benzyl sulfoximines have been previously described, reports of their deprotection are very limited, presumably due to lab

Efficient photoacids based upon triarylamine dialkylsulfonium salts

Zhou, Wenhui,Kuebler, Stephen M.,Carrig, Dave,Perry, Joseph W.,Marder, Seth R.

, p. 1897 - 1901 (2007/10/03)

New triarylamine dialkylsulfonium salts that are photosensitive in the near-ultraviolet have been prepared. The quantum yields of photoacid generation were found to be ～0.5 and are independent of the counterion. On the other hand, the efficiencies of the sulfonium salts toward the photopolymerization of cyclohexene oxide depend on the counterion and the sulfonium substituents. Photopolymerization kinetic studies demonstrate that these triphenylamine sulfonium salts are highly efficient cationic photoinitiators.

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