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85313-85-5

S-(α-chloro-p-nitrobenzyl)-S-phenylsulfoximide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85313-85-5 Structure

  • Basic information

    1. Product Name: S-(α-chloro-p-nitrobenzyl)-S-phenylsulfoximide
    2. Synonyms:
    3. CAS NO:85313-85-5
    4. Molecular Formula:
    5. Molecular Weight: 310.761
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85313-85-5.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: S-(α-chloro-p-nitrobenzyl)-S-phenylsulfoximide(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-(α-chloro-p-nitrobenzyl)-S-phenylsulfoximide(85313-85-5)
    11. EPA Substance Registry System: S-(α-chloro-p-nitrobenzyl)-S-phenylsulfoximide(85313-85-5)

  • 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: 85313-85-5(Hazardous Substances Data)

85313-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85313-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,1 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85313-85:
(7*8)+(6*5)+(5*3)+(4*1)+(3*3)+(2*8)+(1*5)=135
135 % 10 = 5
So 85313-85-5 is a valid CAS Registry Number.

85313-85-5Relevant articles and documents

Halogenations of S-Benzyl-S-phenylsulfoximides and Base-induced Rearrangements of Their N- and α-Halo Derivatives to N-Sulfinylimines

Yoshida, Toyokichi,Naruto, Shunsuke,Uno, Hitoshi,Nishimura, Haruki

, p. 4346 - 4351 (2007/10/02)

The reactions of S-benzyl- and S-(p-nitrobenzyl)sulfoximides 1a, b with N-bromosuccinimide or tert-butyl hypochlorite gave the corresponding N-halosulfoximides 2a, b or 3a, b, respectively, in good yields.The N-bromo-S-(p-nitrobenzyl)sulfoximide 2b decomp

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