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398489-28-6

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398489-28-6 Usage

Explanation

Different sources of media describe the Explanation of 398489-28-6 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. The compound is derived from the esterification of 1-azetidinecarboxylic acid, which is a four-membered heterocyclic compound containing a nitrogen atom.
3. The compound contains an ester functional group, a four-membered nitrogen-containing heterocyclic ring, and a hydroxyl group.
4. It is commonly used in the pharmaceutical industry for the synthesis of various drugs and pharmaceutical intermediates.
5. Due to its unique structure and properties, the compound has potential applications in the fields of medicine and agriculture.
6. It is important to handle this chemical with care, as it may pose health risks if mishandled or incorrectly used.
7. The name follows the IUPAC nomenclature rules and provides information about the structure and functional groups present in the compound.
8. The appearance of the compound (e.g., color, state, etc.) is not mentioned in the provided material.
9. The solubility of the compound in various solvents is not mentioned in the provided material.
10. Information about the stability of the compound under different conditions is not provided in the material.

Structure

Ester of 1-azetidinecarboxylic acid

Functional Groups

Ester, heterocyclic ring, hydroxyl group

Application

Pharmaceutical industry

Potential Applications

Medicine and agriculture

Health Risks

Handle with care

Appearance

Not specified in the material

Solubility

Not specified in the material

Stability

Not specified in the material

Check Digit Verification of cas no

The CAS Registry Mumber 398489-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,4,8 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 398489-28:
(8*3)+(7*9)+(6*8)+(5*4)+(4*8)+(3*9)+(2*2)+(1*8)=226
226 % 10 = 6
So 398489-28-6 is a valid CAS Registry Number.

398489-28-6SDS

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 tert-butyl 3-ethyl-3-hydroxyazetidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-azetidinecarboxylic acid,3-ethyl-3-hydroxy-,1,1-dimethylethyl ester

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:398489-28-6 SDS

398489-28-6Relevant articles and documents

NITROGEN HETEROCYCLIC COMPOUNDS AND METHODS OF USE

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Paragraph 1808; 1909; 2070, (2021/06/26)

The present disclosure relates to compounds of formula (I): and pharmaceutically acceptable salts and stereoisomers thereof. The present disclosure also relates to methods of preparing the compounds, compositions comprising the compounds, and methods of using the compounds as inhibitors of receptor tyrosine kinases, in particular oncogenic mutants of ErbB-receptors e.g. in the treatment of cancer.

SUBSTITUTED DIHYDROPYRAZOLO PYRAZINE CARBOXAMIDE DERIVATIVES

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Page/Page column 83, (2020/01/10)

The invention relates to substituted dihydropyrazolo pyrazine carboxamide derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.

Regiodivergent Stereoselective Access to Fused Alkylideneazetidines

Music, Arif,Baumann, Andreas N.,Eisold, Michael,Didier, Dorian

, p. 783 - 792 (2018/01/28)

Following recent advances in the generalization and simplification of 2H-azetine synthesis, a regiodivergent approach to fused 2- and 3-alkylideneazetines was designed via the intermediate formation of unprecedented vinylazetine structures. Concise sequen

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