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11-<3-(tetrahydro-2-pyranyloxy)propyl>-6,11-dihydrodibenzothiepin-11-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

345941-23-3

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345941-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 345941-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,5,9,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 345941-23:
(8*3)+(7*4)+(6*5)+(5*9)+(4*4)+(3*1)+(2*2)+(1*3)=153
153 % 10 = 3
So 345941-23-3 is a valid CAS Registry Number.

345941-23-3SDS

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 11-[3-(tetrahydro-2-pyranyloxy)propyl]-6,11-dihydrodibenzo[b,e]thiepin-11-carbonitrile

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:345941-23-3 SDS

345941-23-3Downstream Products

345941-23-3Relevant academic research and scientific papers

11-(DIMETHYLAMINOALKYL)-6,11-DIHYDRODIBENZOTHIEPIN-11-CARBONITRILES AND SOME RELATED COMPOUNDS

Sindelar, Karel,Holubek, Jiri,Ryska, Miroslav,Svatek, Emil,Urban, Jiri,Protiva, Miroslav

, p. 1898 - 1909 (2007/10/02)

The title compounds II and III were obtained by alkylations of 6,11-dihydrodibenzothiepin-11-carbonitrile (I) with 2-dimethylaminoethyl chloride and 3-dimethylaminopropyl chloride in the presence of sodium hydride or sodium amide.Hydrolysis of the nitrile II with potassium hydroxide in ethanol resulted in a small amount of the amino acid X and in the amine XI as the main product.Alkylations of I with 1,2-dibromoethane and 1,3-dibromopropane in the presence of sodium hydride gave the bromoalkylnitriles IV and V and the alkylenebisnitriles XIII and XIV.The preparation of the methylpiperazinopropyl derivative VI proved the usefulness of compounds IV and V in the synthesis of further aminonitriles of this series.Alkylation of the nitrile I with 1,2-dibromoethane in the presence of sodium hydroxide or potassium carbonate and benzyltriethylammonium chloride afforded three isomeric nitriles C17H13NS: the vinyl derivative IX, the 6,11-ethano-6H,11H-dibenzothiepin derivative XV and finally the 1a,11b-dihydro-1H,7H-dibenzocyclopropathiocin derivative XVI.Compounds II, III, VI and XII showed some spasmolytic effects but their central neurotropic activity is insignificant.

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