13076-30-7

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• Basic information

  1. Product Name: Anthracene, 1-methoxy-9,10-diphenyl-
  2. Synonyms:
  3. CAS NO:13076-30-7
  4. Molecular Formula: C27H20O
  5. Molecular Weight: 360.455
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13076-30-7.mol
  9. Article Data: 2

• 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: Anthracene, 1-methoxy-9,10-diphenyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Anthracene, 1-methoxy-9,10-diphenyl-(13076-30-7)
  11. EPA Substance Registry System: Anthracene, 1-methoxy-9,10-diphenyl-(13076-30-7)

• 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: 13076-30-7(Hazardous Substances Data)

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13076-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13076-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13076-30:
(7*1)+(6*3)+(5*0)+(4*7)+(3*6)+(2*3)+(1*0)=77
77 % 10 = 7
So 13076-30-7 is a valid CAS Registry Number.

13076-30-7Upstream product

• 2398-37-0 3-methoxyphenyl bromide 
• 873991-74-3 9,10-diphenyl-9,10-dihydro-anthracene-1,9,10-triol 
• 82-39-3 1-methoxyanthracene-9,10-dione 
• 95953-18-7 9,10-Diphenyl-[1]anthrol 
• 77-78-1 dimethyl sulfate 
• 875837-48-2 1-methoxy-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol 

13076-30-7Downstream Products

• 32287-29-9 1-methoxy-9,10-diphenyl-9,10-dihydro-9,10-epidioxido-anthracene 

13076-30-7Relevant articles and documents

Synthesis of 9,10-Diarylanthracenes via Mg(TMP) 2 ·2LiCl-Mediated Benzyne Generation/[4+2] Cycloaddition and Deoxygenation of 9,10-Epoxyanthracene Intermediates

Miyamoto, Naoya,Nakazawa, Yuki,Nakamura, Takanori,Okano, Kentaro,Sato, Sota,Sun, Zhe,Isobe, Hiroyuki,Tokuyama, Hidetoshi

, p. 513 - 518 (2017/12/08)

A new synthetic route to functionalized 9,10-diarylanthracenes has been developed. 9,10-Epoxyanthracene intermediates were prepared by [4+2] cycloaddition of 1,3-diarylisobenzofuran with a variety of functionalized benzyne intermediates, which were obtained by Mg(TMP) 2 ·2LiCl-mediated benzyne generation. For the cleavage of the resultant 9,10-epoxyanthracene intermediates, we developed mild deoxygenation conditions using a combination of trifluoroacetic acid and Et 3 SiH. The utility of this sequence was demonstrated by application to the synthesis of 5,7,12,14-tetraphenylpentacene.

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