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1H-2-Benzothiopyran, 3,4-dihydro-1-(methoxyphenylmethylene)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89805-89-0

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89805-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89805-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89805-89:
(7*8)+(6*9)+(5*8)+(4*0)+(3*5)+(2*8)+(1*9)=190
190 % 10 = 0
So 89805-89-0 is a valid CAS Registry Number.

89805-89-0SDS

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 1-[methoxy(phenyl)methylidene]-3,4-dihydroisothiochromene

1.2 Other means of identification

Product number -
Other names -

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:89805-89-0 SDS

89805-89-0Downstream Products

89805-89-0Relevant academic research and scientific papers

Syntheses and Thermal Reactions of Cyclic Sulphenium Ylides: 2-Alkyl(or aryl)-1-benzoyl-1H-thianaphthalen-2-ium-1-ides and 2-Alkyl(or aryl)-1-benzoyl-3,4-dihydro-1H-2-thianaphthalen-2-ium-1-ides

Kataoka, Tadashi,Tomoto, Akihiko,Shimizu, Hiroshi,Hori, Mikio

, p. 2913 - 2920 (2007/10/02)

Pummerer cyclization of phenacyl phenethyl sulphoxide (5) was carried out using trifluoroacetic anhydride to give 1-benzoyl-3,4-dihydro-1H-2-thianaphthalene (6) in a good yield.Alkylation (or arylation) of 1-benzoyl-1H-2-thianaphthalene (1) and the 3,4-di

SYNTHESIS AND THERMAL REACTIONS OF 2-ALKYL(OR ARYL)-1-BENZOYL-3,4-DIHYDRO-2-THIANAPHTHALENES

Hori, Mikio,Kataoka, Tadashi,Shimizu, Hiroshi,Tomoto, Akihiko

, p. 3629 - 3632 (2007/10/02)

1-Benzoyl-2-methyl-3,4-dihydro-2-thianaphthalene (4a) underwent novel intermolecular 1,4-rearrangement in refluxing toluene to give an enol ether 5a, while rearrangement of 2-phenyl derivative 4e proceeded intramolecularly in refluxing xylene to afford a 1,4-rearranged enol ether 5b.On the other hand, ylides 4a-e were refluxed in alcohols to afford some ring-opened products 10-12.

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