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tert-butyl 2-(hydroxy(pyridin-4-yl)methyl)phenylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126971-79-7

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126971-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126971-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,7 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126971-79:
(8*1)+(7*2)+(6*6)+(5*9)+(4*7)+(3*1)+(2*7)+(1*9)=157
157 % 10 = 7
So 126971-79-7 is a valid CAS Registry Number.

126971-79-7SDS

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 N-{2-[hydroxy(pyridin-4-yl)methyl]-phenyl}-2,2-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names N-[2-(hydroxy-pyridin-4-yl-methyl)-phenyl]-2,2-dimethyl-propionamide

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:126971-79-7 SDS

126971-79-7Relevant academic research and scientific papers

With anti-tumor activity of triazole b the nitrogen is outstanding compound and its preparation method (by machine translation)

-

, (2018/03/24)

The invention discloses a with anti-tumor activity of triazole b the nitrogen is outstanding compound and its preparation method, which belongs to the technical field of medical synthesis. Technical point of the invention is: The invention compared with the prior art has the following advantages: the invention synthetic method is simple, novel and molecular structure can be integrated two nitrogen test paper compound and the triazole compound of the advantages of biological activity, to the breast cancer cell MCF - 7 and liver cancer cell HepG2 inhibition, is expected to be in the direction of the anti-tumor drugs further popularization and application. (by machine translation)

Azacycloheptane-o-diazepine drug molecule with antitumor activity and preparation method thereof

-

, (2018/03/24)

The invention discloses an azacycloheptane-o-diazepine drug molecule with antitumor activity and a preparation method thereof, and belongs to the technical field of medicine synthesis. According to key points of the technical scheme, the novel azacycloheptane-o-diazepine drug molecule disclosed by the invention has the following structure, wherein the structural formula is shown in the specification. The invention further discloses a preparation method of the novel azacycloheptane-o-diazepine drug molecule. The novel azacycloheptane-o-diazepine drug molecule is synthesized according to a novelmethod, the reaction process is simple and feasible in operation, the raw materials are cheap and readily available, and the novel drug molecule is high in reaction efficiency, excellent in repeatability and obvious in antitumor activity and effect.

A novel benzodiazepine three-ring compound and its preparation method and application (by machine translation)

-

, (2018/06/15)

The invention discloses a novel benzodiazepine three-ring compound and its preparation method and application, which belongs to the technical field of medical synthesis. Technical proposal of the invention points are: a novel benzodiazepine three-ring compound, has the following structure: Wherein R is O or S. The invention also discloses a novel benzodiazepine tricyclic compound of the preparation method. The invention a new method to synthesize a novel benzodiazepine three-ring compound, the reaction process is simple and easy operation, the raw material is cheap, environmental protection, higher reaction efficiency and good repeatability, has good anti-platelet aggregation activity and anti-tumor activity. (by machine translation)

4-substituted benzodiazepine 2-one compounds with anti-platelet aggregation activity and supercritical preparation method of 4-substituted benzodiazepine 2-one compounds

-

, (2018/04/26)

The invention discloses 4-substituted benzodiazepine 2-one compounds and a supercritical preparation method thereof, and belongs to the technical field of synthesis of pharmaceutical intermediates. The technical scheme is that the 4-substituted benzodiazepine 2-one compounds have the structure shown in the description, wherein R is methyl, ethyl, propyl, isopropyl, cyclopropyl or cyclohexyl. The invention further discloses the supercritical preparation method of the 4-substituted benzodiazepine 2-one compounds. The 4-substituted benzodiazepine 2-one compounds are synthesized with a novel method, the reaction process is simple and feasible to operate, the raw materials are cheap, easily available and environmentally friendly, the reaction efficiency is higher, and the repeatability is better.

2-amino substituted benzodiarizonaepine compound with antineoplastic activity and preparation method thereof

-

, (2018/05/01)

The invention discloses a 2-amino substituted benzodiarizonaepine compound with antineoplastic activity and a preparation method thereof, and belongs to the technical field of medicine synthesis. Thetechnical character of the compound is shown in the specification, wherein R is CH3, C2H5, C3H7 and phenyl. Compared with the prior art, the compound has the benefits that the synthesis method is simple, the molecular structure is novel, the reaction effect repeatability is good, the compound has inhibiting effect on both breast cancer cell MCF-7 and hepatocarcinoma cell HepG2, and is expected tobe further promoted and applied.

From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novel p38MAP kinase inhibitors

Peifer, Christian,Kinkel, Katrin,Abadleh, Mohammed,Schollmeyer, Dieter,Laufer, Stefan

, p. 1213 - 1221 (2007/10/03)

In this study we describe the design, synthesis, and biological evaluation of 3-(4-fluorophenyl)-4-pyridin-4-ylquinoline-2(1H)-one (5) as a new inhibitor of MAPK with a p38αMAPK IC50 of 1.8 μM. By keeping the common vicinal pyridine/4-F-phenyl

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