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2-[(4-phenylpiperazin-1-yl)methyl]cyclohexanone is a complex organic compound with the molecular formula C20H26N2O. It features a cyclohexanone core, which is a six-membered carbon ring with a ketone group (C=O) at the 2-position. Attached to this core is a 4-phenylpiperazin-1-ylmethyl group, which consists of a piperazine ring (a heterocyclic compound with two nitrogen atoms) substituted at the 4-position with a phenyl group (a benzene ring) and a methyl group. 2-[(4-phenylpiperazin-1-yl)methyl]cyclohexanone is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure allows for the exploration of different chemical properties and interactions, making it a valuable compound in medicinal chemistry research.

735-78-4

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735-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 735-78-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 735-78:
(5*7)+(4*3)+(3*5)+(2*7)+(1*8)=84
84 % 10 = 4
So 735-78-4 is a valid CAS Registry Number.

735-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-phenylpiperazin-1-yl)methyl]cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names MA 1050

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:735-78-4 SDS

735-78-4Downstream Products

735-78-4Relevant academic research and scientific papers

Carbamoyloximes as novel non-competitive mGlu5 receptor antagonists

Galambos, Janos,Wagner, Gabor,Nogradi, Katalin,Bielik, Attila,Molnar, Laszlo,Bobok, Amrita,Horvath, Attila,Kiss, Bela,Kolok, Sandor,Nagy, Jozsef,Kurko, Dalma,Bakk, Monika L.,Vastag, Monika,Saghy, Katalin,Gyertyan, Istvan,Gal, Krisztina,Greiner, Istvan,Szombathelyi, Zsolt,Keser, Gyoergy M.,Domany, Gyoergy

scheme or table, p. 4371 - 4375 (2010/10/02)

Hit-to-lead optimization of a HTS hit led to new carbamoyloxime derivatives. After identification of an advanced hit (8d) the CYP enzyme inhibitory activity of this class of compounds was successfully eliminated. Systematic exploration of different parts of the advanced hit led us to some promising lead compounds with mGluR5 affinities comparable to that of MPEP.

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