Cas 391859-25-9,1,3-Propanedione, 1-[(1S)-2,3-dihydro-1-[1-hydroxy-3-(phenylthio)-2-propynyl]-7-methoxy-1 H-inden-1-yl]-3-[4,5-dimethoxy-2-(phenylmethoxy)phenyl]-

391859-25-9

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Basic information

Product Name: 1,3-Propanedione, 1-[(1S)-2,3-dihydro-1-[1-hydroxy-3-(phenylthio)-2-propynyl]-7-methoxy-1 H-inden-1-yl]-3-[4,5-dimethoxy-2-(phenylmethoxy)phenyl]-
Synonyms:
CAS NO:391859-25-9
Molecular Formula: C37H34O7S
Molecular Weight: 622.739
EINECS: N/A
Product Categories: N/A
Mol File: 391859-25-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1,3-Propanedione, 1-[(1S)-2,3-dihydro-1-[1-hydroxy-3-(phenylthio)-2-propynyl]-7-methoxy-1 H-inden-1-yl]-3-[4,5-dimethoxy-2-(phenylmethoxy)phenyl]-(CAS DataBase Reference)
NIST Chemistry Reference: 1,3-Propanedione, 1-[(1S)-2,3-dihydro-1-[1-hydroxy-3-(phenylthio)-2-propynyl]-7-methoxy-1 H-inden-1-yl]-3-[4,5-dimethoxy-2-(phenylmethoxy)phenyl]-(391859-25-9)
EPA Substance Registry System: 1,3-Propanedione, 1-[(1S)-2,3-dihydro-1-[1-hydroxy-3-(phenylthio)-2-propynyl]-7-methoxy-1 H-inden-1-yl]-3-[4,5-dimethoxy-2-(phenylmethoxy)phenyl]-(391859-25-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 391859-25-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 391859-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,1,8,5 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 391859-25:
(8*3)+(7*9)+(6*1)+(5*8)+(4*5)+(3*9)+(2*2)+(1*5)=189
189 % 10 = 9
So 391859-25-9 is a valid CAS Registry Number.

391859-25-9Upstream product

391859-25-9Downstream Products

391859-25-9Relevant academic research and scientific papers

Enantiodivergent synthesis of either enantiomer of ABCDE-ring analogue of antitumor antibiotic fredericamycin A via intramolecular [4 + 2] cycloaddition approach

Akai, Shuji,Tsujino, Toshiaki,Fukuda, Nobuhisa,Iio, Kiyosei,Takeda, Yoshifumi,Kawaguchi, Ken-Ichi,Naka, Tadaatsu,Higuchi, Kazuhiro,Kita, Yasuyuki

, p. 4015 - 4018 (2007/10/03)

matrix presented An intramolecular enantiodivergent synthesis of both enantiomers of the ABCDE-ring analogue 22 of fredericamycin A is reported. Key steps involved an intramolecular [4 + 2] cycloaddition of 17 and an aromatic Pummerer-type reaction of 19.

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