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795278-07-8

1,3-Benzodioxole-5-carboxaldehyde, 6-bromo-7-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 795278-07-8 Structure

  • Basic information

    1. Product Name: 1,3-Benzodioxole-5-carboxaldehyde, 6-bromo-7-methoxy-
    2. Synonyms:
    3. CAS NO:795278-07-8
    4. Molecular Formula: C9H7BrO4
    5. Molecular Weight: 259.056
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 795278-07-8.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: 1,3-Benzodioxole-5-carboxaldehyde, 6-bromo-7-methoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzodioxole-5-carboxaldehyde, 6-bromo-7-methoxy-(795278-07-8)
    11. EPA Substance Registry System: 1,3-Benzodioxole-5-carboxaldehyde, 6-bromo-7-methoxy-(795278-07-8)

  • 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: 795278-07-8(Hazardous Substances Data)

795278-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 795278-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,5,2,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 795278-07:
(8*7)+(7*9)+(6*5)+(5*2)+(4*7)+(3*8)+(2*0)+(1*7)=218
218 % 10 = 8
So 795278-07-8 is a valid CAS Registry Number.

795278-07-8Relevant articles and documents

Total synthesis of eupomatilones 4 and 6: Structurally rearranged and atropisomerically fluxional lignan natural products

Coleman, Robert S.,Gurrala, Srinivas Reddy

, p. 4025 - 4028 (2004)

(Chemical Equation Presented) A convergent and diastereocontrolled total synthesis of eupomatilones 4 and 6 is reported and was based on a diastereoselective hydroboration/ oxidation sequence and a convergent Lipshutz biarylcuprate cross-coupling reaction. The structure of eupomatilone 6 is revised.

Asymmetric total synthesis of dibenzocyclooctadiene lignan natural products

Coleman, Robert S.,Gurrala, Srinivas Reddy,Mitra, Soumya,Raao, Amresh

, p. 8932 - 8941 (2007/10/03)

Full details of the asymmetric total syntheses of the dibenzocyclooctadiene lignans interiotherin A, angeloylgomisin R, gomisin O, and gomisin E (epigomisin O) are presented. The syntheses were based on a unified synthetic strategy involving a novel crotylation using the Leighton auxiliary that occurred with excellent asymmetric induction (>98:2 enantiomeric ratio), a diastereoselective hydroboration/Suzuki-Miyaura coupling reaction sequence, and an atropdiastereoselective biarylcuprate coupling, both of which occurred with total (>20:1) stereocontrol. The syntheses were achieved in six to eight steps from simple aromatic precursors.

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