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34341-05-4

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34341-05-4 Usage

Description

Cyclopentadecanone oxime is a chemical compound that serves as a reagent in organic synthesis. It is characterized by its oxime functional group, which endows it with reactivity that allows it to participate in a range of chemical reactions, such as hydrolysis to release the parent ketone. CYCLOPENTADECANONE OXIME is also recognized for its potential biological activities, including antimicrobial and antioxidant properties, and it may function as a pharmaceutical intermediate. Cyclopentadecanone oxime plays a multifaceted role in organic chemistry and could have applications in medicine and agriculture.

Uses

Used in Organic Synthesis:
Cyclopentadecanone oxime is used as a reagent for its ability to participate in various chemical reactions, including hydrolysis, which is crucial for the synthesis of different organic compounds.
Used as a Protecting Group:
In the context of organic synthesis, Cyclopentadecanone oxime is used as a protecting group for carbonyl compounds. This role is essential for preventing unwanted side reactions and ensuring the desired product is formed during the synthesis process.
Used in the Preparation of Nitrogen-Containing Compounds:
Cyclopentadecanone oxime serves as a precursor in the preparation of nitrogen-containing compounds, which are vital in various chemical and pharmaceutical applications.
Used in Pharmaceutical Research:
Due to its potential biological activities, Cyclopentadecanone oxime is used in pharmaceutical research as an intermediate. Its antimicrobial and antioxidant properties are of particular interest for the development of new drugs.
Used in Antimicrobial Applications:
Cyclopentadecanone oxime is studied for its antimicrobial properties, which could be harnessed in the development of treatments for bacterial infections.
Used in Antioxidant Applications:
CYCLOPENTADECANONE OXIME's antioxidant properties make it a candidate for use in applications that require protection against oxidative stress, which is implicated in various diseases and conditions.
Used in Agriculture:
Given its potential antimicrobial and antioxidant properties, Cyclopentadecanone oxime may also find applications in agriculture, possibly in the development of pesticides or preservatives to protect crops.

Check Digit Verification of cas no

The CAS Registry Mumber 34341-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34341-05:
(7*3)+(6*4)+(5*3)+(4*4)+(3*1)+(2*0)+(1*5)=84
84 % 10 = 4
So 34341-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H29NO/c17-16-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-15/h17H,1-14H2

34341-05-4SDS

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 N-cyclopentadecylidenehydroxylamine

1.2 Other means of identification

Product number -
Other names N-Hydroxycyclopentadecanimine

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:34341-05-4 SDS

34341-05-4Upstream product

34341-05-4Relevant articles and documents

Chlorination of oximes with aqueous H2O2/HCl system: Facile synthesis of gem-chloronitroso- and gem-chloronitroalkanes, gem-chloronitroso- and gem-chloronitrocycloalkanes

Terent'ev, Alexander O.,Krylov, Igor B.,Ogibin, Yuri N.,Nikishin, Gennady I.

, p. 3819 - 3824 (2008/02/09)

Chlorination of cyclic and linear ketone oximes with aqueous H 2O2/HCl in a two-phase dichloromethane-water system selectively affords gem-chloronitroso compounds in yields of up to 94%. One-pot oxidation of the resulting gem-chloronitroso compounds with peracetic acid, prepared in situ, gives gem-chloronitroalkanes and cycloalkanes in yields of up to 82%. The advantages of the method are that it is facile and environmentally benign and does not require gaseous chlorine. Georg Thieme Verlag Stuttgart.

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