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9-benzyl-9,10-dihydro-8H-7-oxa-9-aza-dibenzo[c,g]phenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1381799-97-8 Structure
  • Basic information

    1. Product Name: 9-benzyl-9,10-dihydro-8H-7-oxa-9-aza-dibenzo[c,g]phenanthrene
    2. Synonyms:
    3. CAS NO:1381799-97-8
    4. Molecular Formula:
    5. Molecular Weight: 375.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1381799-97-8.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: 9-benzyl-9,10-dihydro-8H-7-oxa-9-aza-dibenzo[c,g]phenanthrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-benzyl-9,10-dihydro-8H-7-oxa-9-aza-dibenzo[c,g]phenanthrene(1381799-97-8)
    11. EPA Substance Registry System: 9-benzyl-9,10-dihydro-8H-7-oxa-9-aza-dibenzo[c,g]phenanthrene(1381799-97-8)
  • 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: 1381799-97-8(Hazardous Substances Data)

1381799-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1381799-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,1,7,9 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1381799-97:
(9*1)+(8*3)+(7*8)+(6*1)+(5*7)+(4*9)+(3*9)+(2*9)+(1*7)=218
218 % 10 = 8
So 1381799-97-8 is a valid CAS Registry Number.

1381799-97-8Downstream Products

1381799-97-8Relevant articles and documents

Synthesis of chiral helical 1,3-oxazines

Talele, Harish R.,Sahoo, Sibaprasad,Bedekar, Ashutosh V.

, p. 3166 - 3169 (2012)

A series of novel 1,3-oxazines were prepared to construct a helical framework. The 1,3-oxazine attached to the phenanthrene unit showed a small bite angle θ (~12°), while the units attached to [4]helicene showed a larger θ (~35°) and exhibited helical isomers at ambient conditions. The diastereomers of the third type of helicene-like bis-oxazine attached to binaphthyl were easily separable and showed good thermal stability. All four diastereomers of bis-helicene were synthesized, and their absolute configuration was established.

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