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4H-Thieno[3,2-c]azepin-4-one, 5,6,7,8-tetrahydro- is a heterocyclic compound characterized by a thienoazepine core structure. Thienoazepine is a fused ring system consisting of a thiophene (a benzene ring with one carbon atom replaced by a sulfur atom) and an azepine (a seven-membered ring with one nitrogen atom). The compound is further defined by the presence of a 4-one functional group, indicating a carbonyl group at the 4th position, and a tetrahydro prefix, which signifies the presence of four hydrogen atoms attached to the molecule, resulting in a reduction of the double bonds in the ring system. This specific compound is a member of the azepine family and is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system.

4751-59-1

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4751-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4751-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4751-59:
(6*4)+(5*7)+(4*5)+(3*1)+(2*5)+(1*9)=101
101 % 10 = 1
So 4751-59-1 is a valid CAS Registry Number.

4751-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8-tetrahydro-thieno[3,2-c]azepin-4-one

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:4751-59-1 SDS

4751-59-1Downstream Products

4751-59-1Relevant academic research and scientific papers

p-diaminobenzene derivative as potassium channel regulator, preparation method and medical applications thereof

-

, (2019/12/09)

The invention relates to a p-diaminobenzene derivative as a potassium channel regulator, a preparation method and medical applications thereof, and specifically discloses a compound represented by a general formula A or a pharmaceutically acceptable salt

Visible Light Mediated Aryl Migration by Homolytic C?N Cleavage of Aryl Amines

Alpers, Dirk,Cole, Kevin P.,Stephenson, Corey R. J.

supporting information, p. 12167 - 12170 (2018/09/11)

The photocatalytic preparation of aminoalkylated heteroarenes from haloalkylamides via a 1,4-aryl migration from nitrogen to carbon, conceptually analogous to a radical Smiles rearrangement, is reported. This method enables the substitution of amino group

Regioselective synthesis of several heterocyclic fused azepines using diisobutylaluminum hydride

Cho, Hidetsura,Murakami, Kengo,Nakanishi, Hiroyuki,Isoshima, Hirotaka,Hayakawa, Kazuhide,Uchida, Itsuo

, p. 919 - 927 (2007/10/03)

5,6,7,8-Tetrahydrothieno[3,2-b]azepine,5,6,7,8-tetrahydro-1H-furo[3,2-b] azepine, and 1,4,5,6,7,8-hexahydropyrrolo[3,2-b]azepine were synthesized by the ring expansion reaction of heterocyclic fused cyclohexanone oximes with diisobutylaluminum hydride (DIBAH). The mechanism of the reaction was different from that of Beckmann rearrangement.

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