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CAS

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162147-22-0

Butanedioic acid, [[2-bromo-5-(1-methylethoxy)phenyl]methylene]-, 4-(1,1-dimethylethyl) 1-ethyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162147-22-0 Structure

  • Basic information

    1. Product Name: Butanedioic acid, [[2-bromo-5-(1-methylethoxy)phenyl]methylene]-, 4-(1,1-dimethylethyl) 1-ethyl ester, (E)-
    2. Synonyms:
    3. CAS NO:162147-22-0
    4. Molecular Formula: C20H27BrO5
    5. Molecular Weight: 427.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162147-22-0.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: Butanedioic acid, [[2-bromo-5-(1-methylethoxy)phenyl]methylene]-, 4-(1,1-dimethylethyl) 1-ethyl ester, (E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanedioic acid, [[2-bromo-5-(1-methylethoxy)phenyl]methylene]-, 4-(1,1-dimethylethyl) 1-ethyl ester, (E)-(162147-22-0)
    11. EPA Substance Registry System: Butanedioic acid, [[2-bromo-5-(1-methylethoxy)phenyl]methylene]-, 4-(1,1-dimethylethyl) 1-ethyl ester, (E)-(162147-22-0)

  • 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: 162147-22-0(Hazardous Substances Data)

162147-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162147-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,1,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 162147-22:
(8*1)+(7*6)+(6*2)+(5*1)+(4*4)+(3*7)+(2*2)+(1*2)=110
110 % 10 = 0
So 162147-22-0 is a valid CAS Registry Number.

162147-22-0Relevant articles and documents

Biomimetic total synthesis of michellamines A-C

Bringmann, Gerhard,Goetz, Roland,Harmsen, Sven,Holenz, Joerg,Walter, Rainer

, p. 2045 - 2058 (2007/10/03)

The biomimetic first total synthesis of michellamines A, B, and C (1a-c), naturally occurring quateraryl alkaloids with high anti-HIV activity, is described. Key precursors are the molecular "halves" of michellamines, the antimalarial naphthylisoquinoline

FIRST TOTAL SYNTHESIS OF KORUPENSAMINES A AND B1

Bringmann, Gerhard,Goetz, Roland,Keller, Paul A.,Walter, Rainer,Henschel, Petra,et al.

, p. 503 - 508 (2007/10/02)

The first total synthesis of korupensamines A (1a) and B (1b), highly polar naphthylisoquinoline alkaloids and, simultaneously, 'monomeric building blocks' of the michellamines, is described.Key step is the PdIIcatalyzed intermolecular biaryl coupling of

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