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1314987-79-5

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1314987-79-5 Usage

Description

Tert-butyl3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate is a synthetic organic compound with the chemical formula C12H20N4O4. It belongs to the class of azetidine carboxylates and features a nitro group and pyrazole ring in its structure. This versatile chemical is known for its potential pharmacological properties, including anti-inflammatory and analgesic effects, and is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals due to its reactivity and functional groups. The presence of the tert-butyl group in its structure provides stability and steric hindrance, making it a valuable intermediate in organic synthesis.

Uses

Used in Pharmaceutical Industry:
Tert-butyl3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate is used as a building block for the synthesis of pharmaceuticals due to its versatile reactivity and functional groups. Its potential pharmacological properties, such as anti-inflammatory and analgesic effects, make it a promising candidate for drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical industry, tert-butyl3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate is utilized as a building block for the synthesis of agrochemicals, taking advantage of its reactivity and functional groups to create effective compounds for agricultural applications.
Used in Organic Synthesis:
Tert-butyl3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate is used as a valuable intermediate in organic synthesis, where its tert-butyl group provides stability and steric hindrance, facilitating the creation of complex organic molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1314987-79-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,9,8 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1314987-79:
(9*1)+(8*3)+(7*1)+(6*4)+(5*9)+(4*8)+(3*7)+(2*7)+(1*9)=185
185 % 10 = 5
So 1314987-79-5 is a valid CAS Registry Number.

1314987-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl3-(4-nitro-1H-pyrazol-1-yl)azetidine-1-carboxylate

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:1314987-79-5 SDS

1314987-79-5Downstream Products

1314987-79-5Relevant articles and documents

FGFR Inhibitor compounds and uses thereof

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Paragraph 0487; 0490; 0492-0494, (2021/11/21)

The invention relates to FGFR inhibitor compounds and uses thereof. , The application discloses a compound as shown in a formula (I). A compound, or an optical isomer, a geometric isomer, a tautomer or isomer mixture thereof, or a pharmaceutically acceptable salt thereof, or a prodrug thereof, or a metabolite thereof. The application further relates to the application of the compound in medicine.

INHIBITORS OF NECROPTOSIS

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Page/Page column 37; 38, (2021/09/04)

This invention relates to compounds of Formula (I) and salts, solvates, prodrugs, tautomers, N-oxides, stereoisomers, polymorphs and physiologically functional derivatives thereof. Also disclosed are methods of use of Formula (I), including in the inhibition of necroptosis and treatment of associated diseases, conditions and/or disorders.

BENZAMIDES OF PYRAZOLYL-AMINO-PYRIMIDINYL DERIVATIVES, AND COMPOSITIONS AND METHODS THEREOF

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Paragraph 00362, (2020/07/07)

Provided is a novel class of orally and/or topically available, selective and potent JAK inhibitors as safe and effective therapeutics against various diseases and disorders. More particularly, provided are pharmaceutical composition of these compounds and methods of their preparation and use thereof.

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