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(E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 252377-13-2 Structure
  • Basic information

    1. Product Name: (E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide
    2. Synonyms: (E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide
    3. CAS NO:252377-13-2
    4. Molecular Formula:
    5. Molecular Weight: 335.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 252377-13-2.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: (E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide(252377-13-2)
    11. EPA Substance Registry System: (E)-N-(2-methoxybenzylidene)-P,P-diphenylphosphinic amide(252377-13-2)
  • 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: 252377-13-2(Hazardous Substances Data)

252377-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252377-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,3,7 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 252377-13:
(8*2)+(7*5)+(6*2)+(5*3)+(4*7)+(3*7)+(2*1)+(1*3)=132
132 % 10 = 2
So 252377-13-2 is a valid CAS Registry Number.

252377-13-2Relevant articles and documents

(Thiolan-2-yl)diphenylmethyl benzyl ether/N,N′-diarylurea cocatalyzed asymmetric aziridination of cinnamyl bromide and aryl aldimine

Wang, Shang-Hua,Chein, Rong-Jie

, p. 2607 - 2615 (2016)

A dual catalyst system using THT-based chiral sulfide 2a and H-bond donor 10a was developed for the asymmetric imino Corey-Chaykovsky reaction. Under the optimum reaction conditions, cinnamyl bromide reacted with a wide scope of N-diphenylphosphinic aldim

Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene- based chiral sulfides as organocatalysts

Huang, Meng-Ting,Wu, Hsin-Yi,Chein, Rong-Jie

supporting information, p. 1101 - 1103 (2014/01/17)

This work describes catalytic and asymmetric aziridinations (15 examples, 95-98% ee) of benzyl bromide and imines via the imino Corey-Chaykovsky reaction using (thiolan-2-yl)diarylmethanol benzyl ether as an organocatalyst. The catalyst and analogues thereof were prepared through an expeditious and efficient synthetic route featuring a double nucleophilic substitution and Shi epoxidation as key steps.

Stereoselective synthesis of α-silylamines by the direct addition of silyl anions to activated imines

Ballweg, David M.,Miller, Rebecca C.,Gray, Danielle L.,Scheidt, Karl A.

, p. 1403 - 1406 (2007/10/03)

(Chemical Equation Presented) A highly efficient stereoselective synthesis of unusual α-silylamines via a direct silyl anion addition reaction is reported. This approach is convergent and avoids any problematic aza-Brook shifts of the anionic intermediate

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