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78583-87-6

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78583-87-6 Usage

General Description

3-(4-Bromophenyl)-3-chloroacrylonitrile is a chemical compound that consists of a 3-(4-bromophenyl) group attached to a 3-chloroacrylonitrile group. It is primarily used in the production of pharmaceuticals and agrochemicals. 3-(4-BROMOPHENYL)-3-CHLOROACRYLONITRILE is highly reactive and can act as a versatile building block for the synthesis of various organic molecules. It is also used as an intermediate in the manufacturing of dyes, pigments, and other fine chemicals. However, it is important to handle this compound with caution, as it may pose health and safety risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 78583-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,8 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78583-87:
(7*7)+(6*8)+(5*5)+(4*8)+(3*3)+(2*8)+(1*7)=186
186 % 10 = 6
So 78583-87-6 is a valid CAS Registry Number.

78583-87-6Relevant articles and documents

Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitors

Kumar, Rajiv,Kumar, Amit,Ram, Sita,Angeli, Andrea,Bonardi, Alessandro,Nocentini, Alessio,Gratteri, Paola,Supuran, Claudiu T.,Sharma, Pawan K.

, (2021/10/05)

Two series comprising 20 novel benzenesulfonamides bearing thioureido-linked pyrazole 8 and amino-1,2,4-thiadiazole 10 were synthesized and assayed as human carbonic anhydrase (hCA) inhibitors against isoforms I and II as well as the tumor-associated isof

One-pot synthesis of 2-substituted thieno[3,2-b]indoles from 3-aminothiophene-2-carboxylates through in situ generated 3-aminothiophenes

Irgashev, Roman A.,Steparuk, Alexander S.,Rusinov, Gennady L.

supporting information, (2019/09/30)

A convenient protocol for one-pot synthesis of thieno[3,2-b]indoles, bearing aromatic, thien-2-yl or styryl fragments at C-2 position, from easily accessible 5-substituted 3-aminothiophene-2-carboxylates using the Fischer indolization reaction, was develo

Novel small molecule inhibitors targeting the "switch region" of bacterial RNAP: Structure-based optimization of a virtual screening hit

Sahner, J. Henning,Groh, Matthias,Negri, Matthias,Haupenthal, J?rg,Hartmann, Rolf W.

supporting information, p. 223 - 231 (2013/10/01)

Rising resistance against current antibiotics necessitates the development of antibacterial agents with alternative targets. The "switch region" of RNA polymerase (RNAP), addressed by the myxopyronins, could be such a novel target site. Based on a hit can

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