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4-Phenyl-3a,6a-dihydro-3H-1,2-diaza-4-phospha-pentalene 4-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125657-25-2 Structure
  • Basic information

    1. Product Name: 4-Phenyl-3a,6a-dihydro-3H-1,2-diaza-4-phospha-pentalene 4-oxide
    2. Synonyms:
    3. CAS NO:125657-25-2
    4. Molecular Formula:
    5. Molecular Weight: 218.195
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125657-25-2.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: 4-Phenyl-3a,6a-dihydro-3H-1,2-diaza-4-phospha-pentalene 4-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Phenyl-3a,6a-dihydro-3H-1,2-diaza-4-phospha-pentalene 4-oxide(125657-25-2)
    11. EPA Substance Registry System: 4-Phenyl-3a,6a-dihydro-3H-1,2-diaza-4-phospha-pentalene 4-oxide(125657-25-2)
  • 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: 125657-25-2(Hazardous Substances Data)

125657-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125657-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,6,5 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125657-25:
(8*1)+(7*2)+(6*5)+(5*6)+(4*5)+(3*7)+(2*2)+(1*5)=132
132 % 10 = 2
So 125657-25-2 is a valid CAS Registry Number.

125657-25-2Downstream Products

125657-25-2Relevant articles and documents

REACTIVITY OF CYCLOPENTENYL-ANION ANALOGOUS HETEROCYCLES: SYNTHESIS AND 1,5-ELECTROCYCLISATION OF HOMOPHOSPHOLE

Oebels, Dirk,Klaemer, Frank-Gerrit

, p. 3525 - 3528 (2007/10/02)

The key step of a novel homophosphole synthesis is the reaction of the phospholes 3 with diazomethane in the presence of water leading surprisingly to the oxidized 1,3-dipolar cycloadducts 7.The 1,5-electrocyclization of homophosphole was observed by the racemization of optically active 10c at 120 deg C to be 641 times slower than of homofuran 1a.The activation barrier seems to be largely determined by the barrier of invension at the phosphorus which has to proceed concomitantly.

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