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N-isopropyl-p-trichloroiminophosphorane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37596-20-6 Structure
  • Basic information

    1. Product Name: N-isopropyl-p-trichloroiminophosphorane
    2. Synonyms: N-isopropyl-p-trichloroiminophosphorane
    3. CAS NO:37596-20-6
    4. Molecular Formula:
    5. Molecular Weight: 194.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37596-20-6.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: N-isopropyl-p-trichloroiminophosphorane(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-isopropyl-p-trichloroiminophosphorane(37596-20-6)
    11. EPA Substance Registry System: N-isopropyl-p-trichloroiminophosphorane(37596-20-6)
  • 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: 37596-20-6(Hazardous Substances Data)

37596-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37596-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,9 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37596-20:
(7*3)+(6*7)+(5*5)+(4*9)+(3*6)+(2*2)+(1*0)=146
146 % 10 = 6
So 37596-20-6 is a valid CAS Registry Number.

37596-20-6Upstream product

37596-20-6Downstream Products

37596-20-6Relevant articles and documents

Catalytic double-bond metathesis without the transition metal

Bell, Stephen A.,Meyer, Tara Y.,Geib, Steven J.

, p. 10698 - 10705 (2007/10/03)

Iminophosphoranes of the type X3P=NR (X = CI, pyrrolyl; R = alkyl, aryl) catalytically metathesize C=N bonds of carbodiimides via an addition/elimination mechanism that, despite the lack of d orbital participation in P-N bonding, conserves the key features of metal-catalyzed olefin metathesis. Diazaphosphetidine intermediates, produced by the formal [2 + 2] addition of carbodiimides to the P=N bond, have been isolated and characterized. All phosphorus-containing species in the complex catalytic reaction mixtures have been identified and their origins explained. The kinetics of addition of diisopropylcarbodiimide to Cl3P=NPri and subsequent elimination were studied, and rate constants were determined: kadd 1.7 × 10-3 (±0.1 × 10-3) M s-1 and kelim = 4.0 × 10-4 (±0.3 × 10-4) s-1. The rate of these reactions corresponds well with the observed catalytic TOF of 1.44 TO/P/h.

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