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Benzyl 4-chloropyridin-3-ylcarbamate is an organic compound characterized by the presence of a pyridine ring, a benzyl group, and a carbamate group in its structure. The incorporation of a chlorine atom classifies it as a halogenated compound. Its functional group arrangement makes it a molecule of interest in pharmaceutical or agrochemical fields. Although specific properties such as physical state, color, solubility, melting point, or boiling point are not widely reported, it is likely used as an intermediate or precursor in the synthesis of other compounds. As with many similar compounds, standard safety procedures should be followed during handling to prevent harmful exposure.

1033418-69-7

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1033418-69-7 Usage

Uses

Used in Pharmaceutical Industry:
Benzyl 4-chloropyridin-3-ylcarbamate is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure with a pyridine ring, benzyl group, and carbamate group, along with the halogenated nature, makes it a valuable building block in the development of new drugs.
Used in Agrochemical Industry:
Benzyl 4-chloropyridin-3-ylcarbamate is used as a precursor in the production of agrochemicals, such as pesticides or herbicides. Its structural features contribute to the creation of active ingredients that can be utilized in agricultural applications to control pests and weeds, thereby enhancing crop yield and quality.

Check Digit Verification of cas no

The CAS Registry Mumber 1033418-69-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,4,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1033418-69:
(9*1)+(8*0)+(7*3)+(6*3)+(5*4)+(4*1)+(3*8)+(2*6)+(1*9)=117
117 % 10 = 7
So 1033418-69-7 is a valid CAS Registry Number.

1033418-69-7SDS

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 benzyl N-(4-chloropyridin-3-yl)carbamate

1.2 Other means of identification

Product number -
Other names Benzyl (4-chloropyridin-3-yl)carbamate

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:1033418-69-7 SDS

1033418-69-7Relevant academic research and scientific papers

Design, synthesis and structure activity relationship of potent pan-PIM kinase inhibitors derived from the pyridyl carboxamide scaffold

Nishiguchi, Gisele A.,Burger, Matthew T.,Han, Wooseok,Lan, Jiong,Atallah, Gordana,Tamez, Victoriano,Lindvall, Mika,Bellamacina, Cornelia,Garcia, Pablo,Feucht, Paul,Zavorotinskaya, Tatiana,Dai, Yumin,Wong, Kent

supporting information, p. 2328 - 2332 (2016/04/20)

The Pim proteins (1, 2 and 3) are serine/threonine kinases that have been found to be upregulated in many hematological malignancies and solid tumors. As a result of overlapping functions among the three isoforms, inhibition of all three Pim kinases has become an attractive strategy for cancer therapy. Herein we describe our efforts in identifying potent pan-PIM inhibitors that are derived from our previously reported pyridyl carboxamide scaffold as part of a medicinal chemistry strategy to address metabolic stability.

A modular flow reactor for performing Curtius rearrangements as a continuous flow process

Baumann, Marcus,Baxendale, Ian R.,Ley, Steven V.,Nikbin, Nikzad,Smith, Christopher D.,Tierney, Jason P.

experimental part, p. 1577 - 1586 (2008/10/09)

The use of a mesofluidic flow reactor is described for performing Curtius rearrangement reactions of carboxylic acids in the presence of diphenylphosphoryl azide and trapping of the intermediate isocyanates with various nucleophiles. The Royal Society of Chemistry 2008.

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