Welcome to LookChem.com Sign In|Join Free

CAS

  • or

935662-15-0

(SS)-3-phenylpropyl p-tolyl sulfoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

935662-15-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 935662-15-0 Structure

  • Basic information

    1. Product Name: (SS)-3-phenylpropyl p-tolyl sulfoxide
    2. Synonyms: (SS)-3-phenylpropyl p-tolyl sulfoxide
    3. CAS NO:935662-15-0
    4. Molecular Formula:
    5. Molecular Weight: 258.384
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 935662-15-0.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: (SS)-3-phenylpropyl p-tolyl sulfoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (SS)-3-phenylpropyl p-tolyl sulfoxide(935662-15-0)
    11. EPA Substance Registry System: (SS)-3-phenylpropyl p-tolyl sulfoxide(935662-15-0)

  • 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: 935662-15-0(Hazardous Substances Data)

935662-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 935662-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,6,6 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 935662-15:
(8*9)+(7*3)+(6*5)+(5*6)+(4*6)+(3*2)+(2*1)+(1*5)=190
190 % 10 = 0
So 935662-15-0 is a valid CAS Registry Number.

935662-15-0Relevant articles and documents

Iterative stereospecific reagent-controlled homologation of pinacol boronates by enantioenriched α-chloroalkyllithium reagents

Blakemore, Paul R.,Burge, Matthew S.

, p. 3068 - 3069 (2008/02/05)

Reaction of pinacol boronates with putative enantioenriched α-chloroalkyllithium species, generated in situ from homochiral α-chloroalkylsulfoxides by sulfoxide ligand exchange with t-BuLi in PhMe at -78 °C, gave chain-extended boronic ester products with generally excellent stereochemical fidelity. Iteration of this stereospecific reagent-controlled homologation (StReCH) process enabled the programmed synthesis of all four stereoisomers of a stereodiad-containing model system (4-benzyl-1,6-diphenylhexan-2-ol) with er ≥ 97:3 in all cases. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 935662-15-0