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1447-70-7

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1447-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1447-70-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1447-70:
(6*1)+(5*4)+(4*4)+(3*7)+(2*7)+(1*0)=77
77 % 10 = 7
So 1447-70-7 is a valid CAS Registry Number.

1447-70-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-(1-methyl-4-piperidylidene)-6,11-dihydrodibenzo<b,e>thiepin

1.2 Other means of identification

Product number -
Other names 11-<1-Methyl-piperidyliden-(4)>-6,11-dihydro-dibenz<b,e>thiepin

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:1447-70-7 SDS

1447-70-7Downstream Products

1447-70-7Relevant articles and documents

Piperidine derivative and pharmaceutical composition containing it

-

, (2008/06/13)

Piperidine derivatives of formula (I) and their pharmaceutically acceptable salts have antihypertensive action. The compounds may be included in pharmaceutical compositions for oral or parenteral administration.

POTENTIAL ANTIDEPRESSANTS: SATURATED SIDE CHAIN AMINES DERIVED FROM 6,11-DIHYDRODIBENZOTHIEPIN AND 4,9-DIHYDROTHIENO-2-BENZORHIEPIN

Polivka, Zdenek,Valenta, Vladimir,Sindelar, Karel,Holubek, Jiri,Budesinsky, Milos,et al.

, p. 235 - 247 (2007/10/02)

Reduction of IV with hydroiodic acid afforded almost quantitatively the spirocyclic amino sulfide VII, evidently via V and VI.The carbamate II was chlorinated with N-chlorosuccinimide, the product (XII) was reacted with phenylmagnesium bromide and the reduced with LiAlH4 to give the 6-phenyl derivative X of the antidepressant agent hydrothiadene (I).Treatment of 11-methyl-6,11-dihydrodibenzothiepin (XIII) with butyllithium followed by alkylation with 3-dimethylaminopropyl chloride resulted in 6-(3-dimethylaminopropyl) derivative XIV.Reaction of XIV with ethyl chloroformate and the following alkaline hydrolysis gave the 6-(3-methylaminopropyl) derivative XV (mixture of stereoisomers).Reduction of the corresponding olefinic amine and the tertiary alcohol with hydroiodic acid gave the saturated side chain amines derived from 4,9-dihydrothieno-2-benzothiepin XVIII and XIX.The dihydroderivative of dithiadene XVIII (VUFB-17031) proved very effective in a series of tests predictive of antidepressant activity.

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