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4441-59-2

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4441-59-2 Usage

General Description

4-Cyclohexyl-butylamine is a chemical compound with the molecular formula C10H21N. It is an organic amine with a cyclohexyl and butyl substituent, and is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 4-CYCLOHEXYL-BUTYLAMINE is a clear, colorless liquid with a faint amine odor, and is insoluble in water but soluble in organic solvents such as ethanol and ether. It is also used as a corrosion inhibitor and as a reagent in organic synthesis. Additionally, it has potential applications in the production of polymers and as a surfactant in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 4441-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4441-59:
(6*4)+(5*4)+(4*4)+(3*1)+(2*5)+(1*9)=82
82 % 10 = 2
So 4441-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H21N/c11-9-5-4-8-10-6-2-1-3-7-10/h10H,1-9,11H2

4441-59-2 Well-known Company Product Price

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  • Aldrich

  • (JWP00148)  4-Cyclohexyl-butylamine  AldrichCPR

  • 4441-59-2

  • JWP00148-1G

  • 5,476.77CNY

  • Detail

4441-59-2SDS

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 4-cyclohexylbutan-1-amine

1.2 Other means of identification

Product number -
Other names CYCLOHEXANEBUTANAMINE

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:4441-59-2 SDS

4441-59-2Relevant articles and documents

Anodic benzylic C(sp3)-H amination: Unified access to pyrrolidines and piperidines

Herold, Sebastian,Bafaluy, Daniel,Mu?iz, Kilian

supporting information, p. 3191 - 3196 (2018/07/29)

An electrochemical aliphatic C-H amination strategy was developed to access the important heterocyclic motifs of pyrrolidines and piperidines within a uniform reaction protocol. The mechanism of this unprecedented C-H amination strategy involves anodic C-H activation to generate a benzylic cation, which is efficiently trapped by a nitrogen nucleophile. The applicability of the process is demonstrated for 40 examples comprising both 5- and 6-membered ring formations.

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