Welcome to LookChem.com Sign In|Join Free
  • or
8-benzyl-4,4-bis(4-methoxyphenyl)-12-phenyl-2,3,11-trioxa-8-azatricyclo[4.4.3.0(1,6)]-tridec-12-en-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1042301-86-9

Post Buying Request

1042301-86-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1042301-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042301-86-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,3,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1042301-86:
(9*1)+(8*0)+(7*4)+(6*2)+(5*3)+(4*0)+(3*1)+(2*8)+(1*6)=89
89 % 10 = 9
So 1042301-86-9 is a valid CAS Registry Number.

1042301-86-9Downstream Products

1042301-86-9Relevant academic research and scientific papers

Selective synthesis of trioxapropellanes using manganese(III) acetate

Asahi, Kentaro,Nishino, Hiroshi

, p. 21 - 26 (2008/09/19)

The aerobic oxidation of 2-oxoethyl-substituted cyclic 1,3-dicarbonyl compounds 2, 6, 8 with diarylethenes 1 was carried out in the presence of a catalytic amount of manganese(III) acetate to produce the structurally unique trioxa[4.4.3]propellanes 4,7,9,

Facile endoperoxypropellane synthesis by manganese(III) acetate-mediated aerobic oxidation

Asahi, Kentaro,Nishino, Hiroshi

experimental part, p. 2404 - 2416 (2009/04/10)

Manganese(III)-catalyzed aerobic oxidation of combinations of 3-(2-oxoethyl)piperidine-2,4-diones and 1,1-diarylethenes at room temperature produced structurally interesting trioxaaza[ 4.4.3]propellanes in good yields. Similar reactions using 2-(2-oxoethyl)cyclohexane-1,3-diones also produced the corresponding endoperoxy[4.4.3]propellanes. On the other hand, 3-oxopropyl-substituted cycloalkane-1,3-diones did not give the desired propellanes, 1,2-dioxabicyclic propellane precursors were formed instead in excellent yields. The precursors could be converted into the corresponding propellanes in the presence of a Lewis acid. The mechanism for the formation of the propellanes is also described. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1042301-86-9