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89067-57-2

2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-

    Cas No: 89067-57-2

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  • 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-

    Cas No: 89067-57-2

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  • 89067-57-2 Structure

  • Basic information

    1. Product Name: 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-
    2. Synonyms:
    3. CAS NO:89067-57-2
    4. Molecular Formula: C37H38O6S2
    5. Molecular Weight: 642.837
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89067-57-2.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: 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-(89067-57-2)
    11. EPA Substance Registry System: 2(3H)-Furanone, dihydro-4-[2-[3-methoxy-4-(phenylmethoxy)phenyl]-1,3-dithian-2-yl]-3-[[3 -methoxy-4-(phenylmethoxy)phenyl]methyl]-, trans-(89067-57-2)

  • 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: 89067-57-2(Hazardous Substances Data)

89067-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89067-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89067-57:
(7*8)+(6*9)+(5*0)+(4*6)+(3*7)+(2*5)+(1*7)=172
172 % 10 = 2
So 89067-57-2 is a valid CAS Registry Number.

89067-57-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (benzoxy-4 methoxy-3)benzyl-2(benzoxy-4 methoxy-3 α,α-propylenedithio)benzyl-3 butanolide

1.2 Other means of identification

Product number -
Other names (3S,4S)-3-(4-Benzyloxy-3-methoxy-benzyl)-4-[2-(4-benzyloxy-3-methoxy-phenyl)-[1,3]dithian-2-yl]-dihydro-furan-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89067-57-2 SDS

89067-57-2Relevant articles and documents

ETUDES DE LIGNANES 7 - SYNTHESES TOTALES DES (+-)-α ET -β-CONIDENDRINES ET DES METHYL (+-)-α ET -β-CONIDENDRALS

Dhal, Robert,Nabi, Yahia,Brown, Eric

, p. 2005 - 2016 (2007/10/02)

Michael addition of the carbanion of the dithian 8 on butenolide, followed by alkylation with the benzylic bromide 11 and regeneration of the ketonic carbonyl group, gave the α,β-disubstituted lactone 13.Reduction of the ketonic carbonyl of the latter usi

SYNTHESE TOTALE DE LA (d,l) α-CONIDENDRINE

Nabi, Yahia,Dhal, Robert,Brown, Eric

, p. 1543 - 1546 (2007/10/02)

Michael addition of the carbanion of the dithian 7 (derived from O-benzylvanillin) on butenolide, afforded the saturated lactone 8.Alkylation of the latter with the benzylic bromide 6, followed by regeneration of the carbonyl group gave the α,β-disubstituted lactone 10.Reduction of the ketonic carbonyl group of compound 10 using NaBH4, followed by treatment with CF3CO2H and catalytic hydrogenolysis afforded (d,l)α-conidendrin 1.

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