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4-methyl-N-{(Z)-1-[(pyridin-4-ylmethyl)carbamoyl]-2-thiophen-2-ylethenyl}benzamide is a complex organic compound with a molecular formula of C22H18N2O2S2. It is characterized by a benzamide structure, with a methyl group at the 4-position and a (Z)-1-[(pyridin-4-ylmethyl)carbamoyl]-2-thiophen-2-ylethenyl group attached to the nitrogen atom. 4-methyl-N-{(Z)-1-[(pyridin-4-ylmethyl)carbamoyl]-2-thiophen-2-ylethenyl}benzamide is known for its potential applications in pharmaceutical research, particularly as a chemical intermediate or a precursor in the synthesis of various therapeutic agents. Its structure features a pyridine ring, a thiophene ring, and a carbamoyl group, which contribute to its unique chemical properties and potential interactions with biological targets.

6239-01-6

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6239-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6239-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6239-01:
(6*6)+(5*2)+(4*3)+(3*9)+(2*0)+(1*1)=86
86 % 10 = 6
So 6239-01-6 is a valid CAS Registry Number.

6239-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-dimethyl-4H-benzo[1,4]oxazin-3-one

1.2 Other means of identification

Product number -
Other names 6,8-Dimethyl-4H-benzo[1,4]oxazin-3-one

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:6239-01-6 SDS

6239-01-6Downstream Products

6239-01-6Relevant academic research and scientific papers

Optimization of triazoles as novel and potent nonphlorizin SGLT2 inhibitors

Du, Xiaohui,Lizarzaburu, Mike,Turcotte, Simon,Lee, Taeweon,Greenberg, Joanne,Shan, Bei,Fan, Peter,Ling, Yun,Medina, Julio C.,Houze, Jonathan

, p. 3774 - 3779 (2011/08/06)

Previous efforts have led to the identification of a potent, selective, and nonphlorizin based SGLT2 inhibitor 1. This Letter describes efforts to further optimize the potency, microsomal stability, solubility and pharmacokinetic properties of this series of SGLT2 inhibitors. From these efforts, compounds 28 and 32 have improved solubility and pharmacokinetic properties compared to compound 1.

Carboxylic Acid Compounds and Use Thereof

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Page/Page column 79, (2010/11/28)

Provision of a superior URAT1 activity inhibitor effective for the treatment and the like of a pathology involving uric acid, such as hyperuricemia, gouty tophus, acute gouty arthritis, chronic gouty arthritis, gouty kidney, urinary lithiasis, renal dysfunction, coronary heart disease, ischemic cardiac diseases and the like. A URAT1 activity inhibitor containing a compound represented by the following formula [1] or a pharmaceutically acceptable salt thereof, or a solvate thereof as an active ingredient: [image] wherein each symbol is as defined in the specification.

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