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6,11-Dihydrodibenzo[b,e]thiepine is a heterocyclic organic compound characterized by a unique structure that includes a benzene ring fused to a thiophene ring, with an additional six-membered ring in between. 6,11-dihydrodibenzo[b,e]thiepine is notable for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form complex molecular frameworks. It is a precursor in the production of certain drugs and can be used as an intermediate in organic synthesis. The compound's chemical properties, such as its reactivity and stability, make it a valuable building block in the creation of more complex molecules.

1207-93-8

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1207-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1207-93:
(6*1)+(5*2)+(4*0)+(3*7)+(2*9)+(1*3)=58
58 % 10 = 8
So 1207-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H12S/c1-2-7-13-10-15-14-8-4-3-6-12(14)9-11(13)5-1/h1-8H,9-10H2

1207-93-8SDS

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 6,11-dihydrobenzo[c][1]benzothiepine

1.2 Other means of identification

Product number -
Other names Dibenzo<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:1207-93-8 SDS

1207-93-8Downstream Products

1207-93-8Relevant academic research and scientific papers

Potential Antidepressants. Synthesis of 6,11-Dihydrodibenzothiepin-11-yl 4-(Dimethylaminomethyl)phenyl Ketone and of Some Related Compounds

Metysova, Jirina,Protiva, Miroslav

, p. 1325 - 1330 (2007/10/02)

Reactions of dibenzothiepin-11(6H)-one (4) with 2-, 3- and 4-(dimethylaminomethyl)phenylmagnesium bromide afforded the tertiary alcohols 5a,b,c.The aldehydes 7 and 8 gave similarly the secondary alcohols 9a,b,c and 10c.Numerous attempts to prepare the corresponding ketones, especially by oxidation of 9a,b,c and 10c were unsuccessful.Only the oxidation of 9c with tetrabutylammonium chromate in chloroform afforded the desired ketone 16.Its formation was accompanied by an important side reaction consisting in a cleavage of the "retro-ene-reaction" type leading to compound 11 and the aldehyde 13c which reacted with the chloroform present to give the alcohol 17.Compounds 5a,b,c, 9a,b,c and 16 were tested as potential antidepressants but with the exception of some effects in the test of potentiation of yohimbine toxicity in mice, they proved inactive in this line.

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