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CAS

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862183-13-9

4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 862183-13-9 Structure

  • Basic information

    1. Product Name: 4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine
    2. Synonyms: 4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine
    3. CAS NO:862183-13-9
    4. Molecular Formula:
    5. Molecular Weight: 472.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 862183-13-9.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-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine(862183-13-9)
    11. EPA Substance Registry System: 4-(4-Bromo-phenoxy)-2,6-bis-((S)-4-isopropyl-4,5-dihydro-oxazol-2-yl)-pyridine(862183-13-9)

  • 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: 862183-13-9(Hazardous Substances Data)

862183-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862183-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,1,8 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 862183-13:
(8*8)+(7*6)+(6*2)+(5*1)+(4*8)+(3*3)+(2*1)+(1*3)=169
169 % 10 = 9
So 862183-13-9 is a valid CAS Registry Number.

862183-13-9Relevant articles and documents

A flexible and versatile strategy for the covalent immobilization of chiral catalysts based on pyridinebis(oxazoline) ligands

Cornejo, Alfonso,Fraile, Jose M.,Garcia, Jose I.,Gil, Maria J.,Luis, Santiago V.,Martinez-Merino, Victor,Mayoral, Jose A.

, p. 5536 - 5544 (2007/10/03)

Flexible and versatile methods have been developed for the immobilization of chiral pyridinebis(oxazoline) ligands by covalent bonding to a solid support, either by grafting or by polymerization. Different spacers can easily be introduced to modulate the

Phosphinoselenothioic acids and their salts: Synthesis, characterization, and reaction with electrophiles

Kimura, Tsutomu,Murai, Toshiaki,Miwa, Akihiro,Kurachi, Daisuke,Yoshikawa, Haruhisa,Kato, Shinzi

, p. 5611 - 5617 (2007/10/03)

Phosphinoselenothioic acid ammonium salts were synthesized in good yields by reacting phosphinoselenothioic acid S-[2-(trimethylsilyl)ethyl] esters with ammonium fluorides. Phosphinoselenothioic acid alkali metal salts were obtained as 18-crown-6 ether co

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