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Phosphorane, (4-methylpentylidene)triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54517-55-4 Structure
  • Basic information

    1. Product Name: Phosphorane, (4-methylpentylidene)triphenyl-
    2. Synonyms:
    3. CAS NO:54517-55-4
    4. Molecular Formula: C24H27P
    5. Molecular Weight: 346.452
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54517-55-4.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: Phosphorane, (4-methylpentylidene)triphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphorane, (4-methylpentylidene)triphenyl-(54517-55-4)
    11. EPA Substance Registry System: Phosphorane, (4-methylpentylidene)triphenyl-(54517-55-4)
  • 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: 54517-55-4(Hazardous Substances Data)

54517-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54517-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,1 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54517-55:
(7*5)+(6*4)+(5*5)+(4*1)+(3*7)+(2*5)+(1*5)=124
124 % 10 = 4
So 54517-55-4 is a valid CAS Registry Number.

54517-55-4Relevant articles and documents

A MODEL FOR TRITERPENE SIDE-CHAIN SYNTHESIS

Gibson, Joseph R.,Reusch, William

, p. 55 - 59 (1983)

Although the hindered CO function in trans-1,6-dimethyl-2-methoxybicyclononan-7-one (1) resists nucleophilic addition and is prone to enolate formation, good yields of addition products from trimethylsilyl cyanide, methylenetriphenylphosphorane and

GLYCALS IN STEREOSPECIFIC SYNTHESIS. I. SYNTHESIS OF (+)-cis-DISPARLURE - THE SEX PHEROMONE OF THE GYPSY MOTH (Porthetria dispar L.)

Tolstikov, A. G.,Khakhalina, N. V.,Odinokov, V. N.,Khalilov, L. M.,Spirikhin L. V.

, p. 263 - 268 (2007/10/02)

An original approach to the synthesis of 2R,3S-epoxy-1-hydroxytridecane was developed on the basis of tri-O-acetyl-D-galactal.The product was used as the key synthon in the production of a sample of (+)-cis-disparlure with high optical purity.

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