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Pyridine, 3-cyclopropyl(9CI) is a chemical compound with the formula C7H9N. It is a derivative of pyridine featuring a cyclopropyl group attached to the third carbon atom, forming a three-membered ring. Pyridine, 3-cyclopropyl(9CI) is recognized for its unique structure and diverse reactivity, which makes it a valuable building block in organic synthesis. It is commonly found in pharmaceuticals, agrochemicals, and materials, playing a crucial role in the development of new chemical compounds. However, due to its potential toxicity and flammability, careful handling is required.

188918-72-1

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188918-72-1 Usage

Uses

Used in Pharmaceutical Industry:
Pyridine, 3-cyclopropyl(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Pyridine, 3-cyclopropyl(9CI) serves as a vital component in the creation of pesticides and other agrochemical products. Its reactivity and structural features enable the design of effective compounds for crop protection and enhancement of agricultural yields.
Used in Materials Science:
Pyridine, 3-cyclopropyl(9CI) is utilized in materials science for the development of novel materials with specific properties. Its incorporation into polymers and other materials can lead to improved characteristics such as stability, conductivity, or specific binding affinities, broadening the scope of material applications.
Used in Organic Synthesis:
As a building block in organic synthesis, Pyridine, 3-cyclopropyl(9CI) is employed for the construction of complex organic molecules. Its diverse reactivity allows chemists to create a wide array of compounds for various applications, including the synthesis of natural products, pharmaceuticals, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 188918-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,9,1 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 188918-72:
(8*1)+(7*8)+(6*8)+(5*9)+(4*1)+(3*8)+(2*7)+(1*2)=201
201 % 10 = 1
So 188918-72-1 is a valid CAS Registry Number.

188918-72-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclopropylpyridine

1.2 Other means of identification

Product number -
Other names -

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:188918-72-1 SDS

188918-72-1Downstream Products

188918-72-1Relevant articles and documents

Facile synthesis of aryl(het)cyclopropane catalyzed by palladacycle

Zhang, Min,Cui, Xiuling,Chen, Xiaopei,Wang, Lianhui,Li, Jingya,Wu, Yusheng,Hou, Lifen,Wu, Yangjie

experimental part, p. 900 - 905 (2012/02/01)

Sphos (2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′- biphenyl) adduct of cyclopalladated ferrocenylimine (IIe) exhibited highly catalytic activity for the Suzuki cross-coupling reaction of cyclopropylboronic acid with aryl(het) halides with 1 mol % catalyst loading. This process was applied to both of aryl and heteroaryl halides (Br and Cl), and made the various arylcyclopropane and heteroarylcyclopropane to be easily synthesized. A variety of substituents on the aryl halides, such as alkyl, acetyl, benzoyl, ether, formyl, carboxylate, methoxy, nitro and cyano were tolerated.

Cyclopropylboronic acid: Synthesis and Suzuki cross-coupling reactions

Wallace, Debra J.,Chen, Cheng-Yi

, p. 6987 - 6990 (2007/10/03)

An efficient synthesis of cyclopropylboronic acid is reported. This compound undergoes efficient Suzuki-type coupling reactions with a range of aryl and heteroarybromides.

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