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  • 42016-15-9 Structure
  • Basic information

    1. Product Name: Eupomatenoid 8
    2. Synonyms: Eupomatenoid 8
    3. CAS NO:42016-15-9
    4. Molecular Formula: C20H20O4
    5. Molecular Weight: 324.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 42016-15-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Eupomatenoid 8(CAS DataBase Reference)
    10. NIST Chemistry Reference: Eupomatenoid 8(42016-15-9)
    11. EPA Substance Registry System: Eupomatenoid 8(42016-15-9)
  • 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: 42016-15-9(Hazardous Substances Data)

42016-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42016-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,1 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42016-15:
(7*4)+(6*2)+(5*0)+(4*1)+(3*6)+(2*1)+(1*5)=69
69 % 10 = 9
So 42016-15-9 is a valid CAS Registry Number.

42016-15-9Downstream Products

42016-15-9Relevant articles and documents

Synthesis of (±)-licarin B and eupomatenoids-1 and -12: A general approach to 2-aryl-7-alkoxy-benzofuranoid neolignans

Engler, Thomas A.,Chai, Wenying

, p. 6969 - 6970 (2007/10/03)

New synthesis of the title compounds are described using Lewis acid-promoted reactions of styrenes with N-phenylsulfonyl-1,4-benzoquinone monoimines to regioselectively form the 2-arylbenzofuranoid ring system followed by conversion of the aromatic N-phenylsulfonyl moiety into a propenyl substituent.

A regioselective lithiation of ortho-cresols using the bis(dimethylamino)phosphoryl group as a directing group: General synthesis of 2,3-dihydrobenzo[b]furans including naturally occurring neolignans

Watanabe,Kawanishi,Akiyoshi,Furukawa

, p. 3123 - 3131 (2007/10/02)

A general synthetic method was developed for 2-aryl-2,3-dihydrobenzo[b]furans via regioselective lithiation of ortho-tolyl tetramethylphosphorodiamidates followed by addition of aromatic aldehydes as a key step. ortho-Tolyl tetramethylphosphorodiamidates

NEOLIGNANS FROM MAGNOLIA KACHIRACHIRAI

Ito, Kazuo,Ichino, Kazuhiko,Iida, Toshiyuki,Lai, Jengshiow

, p. 2643 - 2646 (2007/10/02)

Two new neolignans named kachirachirol-A and B were isolated from the leaves of Magnolia kachirachirai and their chemical structures determined to be 2-(p-hydroxyphenyl)-7-methoxy-3-methyl-5-trans-propenylbenzofuran and rel-(2S,3S)-2-catechyl-2,3-dihydro-7-methoxy-3-methyl-5-trans-propenylbenzofuran.Key Word Index - Magnolia kachirachirai; Magnoliaceae; neolignan; benzofuranoid; kachirachirol-A; kachirachirol-B; licarin-A; eupomatenoid.

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