Welcome to LookChem.com Sign In|Join Free
  • or
5-[N-(3',5'-BISTRIFLUOROMETHYLBENZYL)AMINO]-2-METHYLTETRAZOLE is a tetrazole-based organic compound with a unique structure featuring a five-membered tetrazole ring containing four nitrogen atoms and one carbon atom. It also has an amino group attached to a benzyl group, which is substituted with trifluoromethyl groups. These functional groups endow the compound with distinctive chemical properties, making it a promising candidate for applications in medicinal chemistry and the development of pharmaceuticals and bioactive compounds.

669080-86-8

Post Buying Request

669080-86-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

669080-86-8 Usage

Uses

Used in Pharmaceutical Industry:
5-[N-(3',5'-BISTRIFLUOROMETHYLBENZYL)AMINO]-2-METHYLTETRAZOLE is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and potential to enhance the bioactivity and efficacy of drug molecules.
Used in Medicinal Chemistry Research:
5-[N-(3',5'-BISTRIFLUOROMETHYLBENZYL)AMINO]-2-METHYLTETRAZOLE serves as a valuable compound in medicinal chemistry research, where it can be utilized to explore new drug targets, design novel bioactive molecules, and improve the pharmacokinetic and pharmacodynamic properties of existing drugs.
Used in Drug Development:
5-[N-(3',5'-BISTRIFLUOROMETHYLBENZYL)AMINO]-2-METHYLTETRAZOLE is employed in drug development as a building block for creating new chemical entities with potential therapeutic applications, taking advantage of its unique structural features and chemical reactivity.
Used in Bioactive Compounds Synthesis:
5-[N-(3',5'-BISTRIFLUOROMETHYLBENZYL)AMINO]-2-METHYLTETRAZOLE is used as a starting material in the synthesis of bioactive compounds, leveraging its distinctive chemical properties to develop new molecules with potential applications in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 669080-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,0,8 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 669080-86:
(8*6)+(7*6)+(6*9)+(5*0)+(4*8)+(3*0)+(2*8)+(1*6)=198
198 % 10 = 8
So 669080-86-8 is a valid CAS Registry Number.

669080-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[3,5-bis(trifluoromethyl)phenyl]methyl]-2-methyltetrazol-5-amine

1.2 Other means of identification

Product number -
Other names M-1185

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:669080-86-8 SDS

669080-86-8Relevant academic research and scientific papers

Design, synthesis and biological evaluation of n,n-substituted amine derivatives as cholesteryl ester transfer protein inhibitors

Wang, Xinran,Hao, Lijuan,Xu, Xuanqi,Li, Wei,Liu, Chunchi,Zhao, Dongmei,Cheng, Maosheng

, (2017)

N,N-Substituted amine derivatives were designed by utilizing a bioisosterism strategy. Consequently, twenty-two compounds were synthesized and evaluated for their inhibitory activity against CETP. Structure-activity relationship (SAR) studies indicate tha

Development of safe and scalable continuous-flow methods for palladium-catalyzed aerobic oxidation reactions

Ye, Xuan,Johnson, Martin D.,Diao, Tianning,Yates, Matthew H.,Stahl, Shannon S.

scheme or table, p. 1180 - 1186 (2010/10/20)

The synthetic scope and utility of Pd-catalyzed aerobic oxidation reactions has advanced significantly over the past decade, and these reactions have the potential to address important green-chemistry challenges in the pharmaceutical industry. This potential has not been realized, however, because safety concerns and process constraints hinder large-scale applications of this chemistry. These limitations are addressed by the development of a continuous-flow tube reactor, which has been demonstrated on several scales in the aerobic oxidation of alcohols. Use of a dilute oxygen gas source (8% O2 in N 2) ensures that the oxygen/organic mixture never enters the explosive regime, and efficient gas-liquid mixing in the reactor minimizes decomposition of the homogeneous catalyst into inactive Pd metal. These results provide the basis for large-scale implementation of palladium-catalyzed (and other) aerobic oxidation reactions for pharmaceutical synthesis. The Royal Society of Chemistry 2010.

HETEROCYCLIC DERIVATIVES AS CETP INHIBITORS

-

Page/Page column 45-46, (2008/12/05)

The present invention provides a compound of formula (I), said compound is an inhibitor of CETP, and thus can be employed for the treatment of a disorder or disease mediated by CETP or responsive to the inhibition of CETP.

ORGANIC COMPOUNDS

-

Page/Page column 44, (2008/12/05)

The present invention provides a compound of formula (I), said compound is an inhibitor of CETP, and thus can be employed for the treatment of a disorder or disease mediated by CETP or responsive to the inhibition of CETP.

BICYCLIC DERIVATIVES AS CETP INHIBITORS

-

, (2008/06/13)

The present invention relates to novel compounds of formula (I): or a pharmaceutical composition thereof, with all the variables being defined in the text. The present invention further relates to the use of the compounds herein for treatment of or delay

CHOLESTERYL ESTER TRANSFER PROTEIN INHIBITORS

-

Page/Page column 32, (2008/06/13)

Compounds of Formula (I), including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formula

Dibenzyl Amine Compounds and Derivatives

-

Page/Page column 37, (2010/11/28)

Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases in some mammals, including humans.

PYRIDINYL AMINE DERIVATIVES AS INHIBITORS OF CHOLESTERYL ESTER TRANSFER PROTEIN (CETP)

-

Page/Page column 101, (2008/06/13)

The present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein the variables are as defined, useful as inhibitors of chlosteryl ester transfer protein.

Dibenzyl Amine Compounds and Derivatives

-

Page/Page column 34, (2010/11/28)

Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid le

DIBENZYL AMINE COMPOUNDS AND DERIVATIVES

-

Page/Page column 57, (2008/06/13)

Dibenzyl amine compounds and derivatives, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid le

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 669080-86-8