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143438-91-9

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143438-91-9 Usage

General Description

3-Amino-3-[3-(trifluoromethyl)phenyl]propanoic acid is a chemical compound with the molecular formula C10H12F3NO2. It is an amino acid derivative with a trifluoromethylphenyl group attached to the third carbon atom of the propanoic acid chain. 3-Amino-3-[3-(trifluoromethyl)phenyl]propanoic acid has various applications in the field of medicinal chemistry, particularly in the development of drugs targeting neurological and psychiatric disorders. It has been studied as a potential antagonist of the glutamate receptors, which are involved in the pathophysiology of schizophrenia and other mental illnesses. Additionally, its unique chemical structure and properties make it a valuable building block for the synthesis of diverse organic compounds for pharmaceutical and agrochemical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 143438-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,3 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143438-91:
(8*1)+(7*4)+(6*3)+(5*4)+(4*3)+(3*8)+(2*9)+(1*1)=129
129 % 10 = 9
So 143438-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10F3NO2/c11-10(12,13)7-3-1-2-6(4-7)8(14)5-9(15)16/h1-4,8H,5,14H2,(H,15,16)

143438-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-3-[3-(trifluoromethyl)phenyl]-propanoic acid

1.2 Other means of identification

Product number -
Other names 3-Amino-3-[3-(trifluoromethyl)phenyl]propanoic acid

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:143438-91-9 SDS

143438-91-9Relevant articles and documents

Iridium-catalysed C-H borylation of β-aryl-aminopropionic acids

MacDonald, Simon J. F.,Nortcliffe, Andrew,Robinson, Henry,Simelis, Klemensas,Stillibrand, Joe

supporting information, p. 6696 - 6701 (2020/09/21)

Iridium-catalysed catalytic, regioselective C-H borylation of β-aryl-aminopropionic acid derivatives gives access to 3,5-functionalised protected β-aryl-aminopropionic acid boronates. The synthetic versatility of these new boronates is demonstrated through sequential one-pot functionalisation reactions to give diverse building blocks for medicinal chemistry. The C-H borylation is also effective for dipeptide substrates. We have exemplified this methodology in the synthesis of a pan αv integrin antagonist.

BENZIMIDAZOLE DERIVATIVES USEFUL AS POTASSIUM CHANNEL INHIBITORS

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Page/Page column 61, (2019/03/12)

The present invention relates to compounds of the general formula (I). The compounds of formula I are potassium channel inhibitors useful for treatment of a cardiac disease, disorder or condition in a mammal.

NOVEL POTASSIUM CHANNEL INHIBITORS

-

Page/Page column 65, (2017/09/15)

The present invention relates to a compound of the general formula (I). The compounds of formula (I) are useful for treatment of a cardiac disease, disorder or condition in a mammal.

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