Welcome to LookChem.com Sign In|Join Free
  • or
(2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is a chemical compound characterized by the presence of a carbamic acid group and a tert-butyl ester group attached to a phenyl ring, which features an amino and trifluoromethyl substituent. (2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is recognized for its reactivity and potential toxicity, necessitating careful handling and storage. It serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, with the capacity to react with other chemicals to form new compounds and act as a building block for more complex organic molecules.

579474-48-9

Post Buying Request

579474-48-9 Suppliers

Recommended suppliers

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

579474-48-9 Usage

Uses

Used in Pharmaceutical Industry:
(2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its reactivity allows for the formation of diverse compounds with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical sector, (2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is utilized as a precursor in the production of pesticides and other agrochemicals. Its role in creating new compounds aids in enhancing crop protection and management strategies.
Used in Organic Synthesis:
(2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is employed as a building block in organic synthesis, enabling the creation of more complex organic molecules for a wide range of applications, including materials science, specialty chemicals, and research compounds.
Used in Research and Development:
(2-AMINO-4-TRIFLUOROMETHYL-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER is also used in research and development settings to explore its reactivity and potential applications in various chemical reactions, providing insights into new synthetic pathways and chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 579474-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,9,4,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 579474-48:
(8*5)+(7*7)+(6*9)+(5*4)+(4*7)+(3*4)+(2*4)+(1*8)=219
219 % 10 = 9
So 579474-48-9 is a valid CAS Registry Number.

579474-48-9SDS

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 tert-butyl N-[2-amino-4-(trifluoromethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-amino-4-trifluorophenylcarbamate

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:579474-48-9 SDS

579474-48-9Downstream Products

579474-48-9Relevant academic research and scientific papers

NOVEL BENZODIAZEPINONES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR FUNCTIONS AND NEUROLOGICAL USES THEREOF

-

Paragraph 0133; 0134; 0136, (2013/03/28)

The present invention relates to novel benzodiazepinone compounds of Formulae (I) wherein R1, R2, R4, R6, R7, R8, R9, and R10 are as defined herein. The invention also

2-Benzimidazolyl-9-(chroman-4-yl)-purinone derivatives as JAK3 inhibitors

Cole, Andrew G.,Bohnstedt, Adolph C.,Paradkar, Vidyadhar,Kingsbury, Celia,Quintero, Jorge G.,Park, Haengsoon,Lu, Yingchun,You, Ming,Neagu, Irina,Diller, David J.,Letourneau, Jeffrey J.,Shao, Yuefei,James, Ray A.,Riviello, Christopher M.,Ho, Koc-Kan,Lin, Tsung H.,Wang, Bojing,Appell, Kenneth C.,Sills, Matthew,Quadros, Elizabeth,Kimble, Earl F.,Ohlmeyer, Michael H.J.,Webb, Maria L.

scheme or table, p. 6788 - 6792 (2010/06/12)

A novel class of Janus tyrosine kinase 3 (JAK3) inhibitors based on a 2-benzimidazoylpurinone core structure is described. Through substitution of the benzimidazoyl moiety and optimization of the N-9 substituent of the purinone, compound 24 was identified incorporating a chroman-based functional group. Compound 24 shows excellent kinase activity, good oral bioavailability and demonstrates efficacy in an acute mechanistic mouse model through inhibition of interleukin-2 (IL-2) induced interferon-γ (INF-γ) production.

Dihydro-benzo[b][1,4]diazepin-2-one derivatives

-

, (2008/06/13)

This invention relates to dihydro-benzo[b][1,4]diazepin-2-one derivatives of the formula wherein R1, R2, X and Y are as defined in the specification and R3 is a six-membered aromatic heterocycle containing 1 to 3 nitrogen atoms or a pyridine-N-oxide as further defined in the specification. The invention further relates to medicaments containing these compounds, a process for their preparation as well as their use for preparation of medicaments for the treatment or prevention of acute and/or chronic neurological disorders.

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 579474-48-9