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1340597-83-2

C23H27F3O7 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1340597-83-2 Structure

  • Basic information

    1. Product Name: C23H27F3O7
    2. Synonyms:
    3. CAS NO:1340597-83-2
    4. Molecular Formula:
    5. Molecular Weight: 472.458
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1340597-83-2.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: C23H27F3O7(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H27F3O7(1340597-83-2)
    11. EPA Substance Registry System: C23H27F3O7(1340597-83-2)

  • 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: 1340597-83-2(Hazardous Substances Data)

1340597-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1340597-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,0,5,9 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1340597-83:
(9*1)+(8*3)+(7*4)+(6*0)+(5*5)+(4*9)+(3*7)+(2*8)+(1*3)=162
162 % 10 = 2
So 1340597-83-2 is a valid CAS Registry Number.

1340597-83-2Downstream Products

1340597-83-2Relevant articles and documents

Phenolic constituents of Acorus gramineus

Park, Cheol Hyeong,Kim, Ki Hyun,Lee, Il Kyun,Lee, Seung Young,Choi, Sang Un,Lee, Jei Hyun,Lee, Kang Ro

, p. 1289 - 1296 (2011)

The purification of a MeOH extract from the rhizome of Acorus gramineus (Araceae) using column chromatography furnished two new stereoisomers of phenylpropanoid, acoraminol A (1) and acoraimol B (2). It also furnished 17 known phenolic compounds, β-asarone (3), asaraldehyde (4), isoacoramone (5), propioveratrone (6), (1'R,2'S)-1',2'-dihydroxyasarone (7), (1'S,2'S)- 1',2'-dihydroxyasarone (8), 3',4'-dimethoxycinnamyl alcohol (9), 3',4',5'-trimethoxycinnamyl alcohol (10), kaempferol 3-methyl ether (11), 2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]-1,3- propanediol (12), hydroxytyrosol (13), tyrosol (14), (2S,5S)-diveratryl-(3R,4S)-dimethyltetrahydrofuran (15), (7S,8R)-dihydrodehydrodiconiferyl alcohol (16), 7S,8S-threo-4,7,9,9'- tetrahydroxy-3,3'-dimethoxy-8-O-4'-neolignan (17), 7S,8R-erythro-4,7,9,9'- tetrahydroxy-3,3'-dimethoxy-8-O-4'-neolignan (18), and dihydroyashsbushiketol (19). The structures of the new compounds were elucidated by analysis of spectroscopic data including 1D and 2D NMR data. The absolute configurations of 1 and 2 were determined using the convenient Mosher ester procedure. Compounds 5-19 were isolated for the first time from this plant source. The isolated compounds were tested for cytotoxicity against four human tumor cell lines in vitro using a Sulforhodamine B (SRB) bioassay.

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