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CAS

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1268827-88-8

6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268827-88-8 Structure

  • Basic information

    1. Product Name: 6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime
    2. Synonyms: 6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime
    3. CAS NO:1268827-88-8
    4. Molecular Formula:
    5. Molecular Weight: 367.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268827-88-8.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: 6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime(1268827-88-8)
    11. EPA Substance Registry System: 6-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-2,3-dimethoxybenzaldehyde O-methyloxime(1268827-88-8)

  • 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: 1268827-88-8(Hazardous Substances Data)

1268827-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268827-88-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,8,2 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1268827-88:
(9*1)+(8*2)+(7*6)+(6*8)+(5*8)+(4*2)+(3*7)+(2*8)+(1*8)=208
208 % 10 = 8
So 1268827-88-8 is a valid CAS Registry Number.

1268827-88-8Relevant articles and documents

Total synthesis of benzo[c]phenanthridine alkaloids based on a microwave-assisted electrocyclic reaction of the aza 6π-electron system and structural revision of broussonpapyrine

Ishihara, Yuhsuke,Azuma, Shuhei,Choshi, Tominari,Kohno, Kakujirou,Ono, Kanako,Tsutsumi, Hiroyuki,Ishizu, Takashi,Hibino, Satoshi

, p. 1320 - 1333 (2011/04/16)

Total syntheses of the des-N-methyl (nor) type of benzo[c]phenanthridine alkaloids 1a-f and 19 and benzo[c]phenanthridine alkaloids, chelerythrine (2d), and broussonpapyrine (2f) were achieved. The key step was the construction of tetracyclic 10,11-dihydrobenzo[c]phenanthridines using a microwave-assisted electrocyclic reaction of the 2-cycloalkenylbenzaldoxime methyl ether 4 as an aza 6π-electron system, which was derived in two steps from a Suzuki-Miyaura cross-coupling reaction of 2-bromobenzaldehyde 6 with 2-(3,4-dihydro-6,7- methylenedioxynaphthyl)boronic acid pinacol ester 7. In addition, the exact structure of broussonpapyrine (2f) (2,3,9,10-tetraoxygenated type) was determined to be chelerythrine (2d).

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