Welcome to LookChem.com Sign In|Join Free

CAS

  • or

182565-31-7

4-nitro-N-(3-phenylpropyl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182565-31-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 182565-31-7 Structure

  • Basic information

    1. Product Name: 4-nitro-N-(3-phenylpropyl)benzenesulfonamide
    2. Synonyms: 4-nitro-N-(3-phenylpropyl)benzenesulfonamide
    3. CAS NO:182565-31-7
    4. Molecular Formula: C15H16N2O4S
    5. Molecular Weight: 320.36354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182565-31-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-nitro-N-(3-phenylpropyl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-nitro-N-(3-phenylpropyl)benzenesulfonamide(182565-31-7)
    11. EPA Substance Registry System: 4-nitro-N-(3-phenylpropyl)benzenesulfonamide(182565-31-7)

  • 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: 182565-31-7(Hazardous Substances Data)

182565-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182565-31-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,5,6 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 182565-31:
(8*1)+(7*8)+(6*2)+(5*5)+(4*6)+(3*5)+(2*3)+(1*1)=147
147 % 10 = 7
So 182565-31-7 is a valid CAS Registry Number.

182565-31-7Downstream Products

182565-31-7Relevant articles and documents

Practical Intermolecular Hydroarylation of Diverse Alkenes via Reductive Heck Coupling

Gurak, John A.,Engle, Keary M.

, p. 8987 - 8992 (2018/09/11)

The hydroarylation of alkenes is an attractive approach to construct carbon-carbon (C-C) bonds from abundant and structurally diverse starting materials. Herein we report a palladium-catalyzed reductive Heck hydroarylation of aliphatic and heteroatom-substituted terminal alkenes and select internal alkenes with an array of (hetero)aryl iodides. The reaction is anti-Markovnikov selective with terminal alkenes and tolerates a wide variety of functional groups on both the alkene and (hetero)aryl coupling partners. Additionally, applications of this method to complex molecule diversifications are demonstrated. Mechanistic experiments are consistent with a mechanism in which the key alkylpalladium(II) intermediate is intercepted with formate and undergoes a decarboxylation/C-H reductive elimination cascade to afford the saturated product and turn over the cycle.

Designing Homogeneous Bromine Redox Catalysis for Selective Aliphatic C?H Bond Functionalization

Becker, Peter,Duhamel, Thomas,Martínez, Claudio,Mu?iz, Kilian

supporting information, p. 5166 - 5170 (2018/03/28)

The potential of homogeneous oxidation catalysis employing bromine has remained largely unexplored. We herein show that the combination of a tetraalkylammonium bromide and meta-chloroperbenzoic acid offers a unique catalyst system for the convenient and s

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 182565-31-7