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2184-86-3

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2184-86-3 Usage

General Description

"(2R)-2-(2,4-dichlorophenyl)pentanenitrile" is a chemical compound with the molecular formula C12H13Cl2N. It is a chiral molecule, meaning it has two possible mirror-image forms, known as enantiomers. The compound contains a pentanenitrile group, which is a five-carbon chain with a nitrile functional group at one end. Additionally, it has a 2,4-dichlorophenyl group attached to the second carbon atom. This chemical is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It may also have applications in organic chemistry research and as a building block in the production of other complex compounds. Overall, "(2R)-2-(2,4-dichlorophenyl)pentanenitrile" has important industrial and scientific uses due to its unique structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 2184-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2184-86:
(6*2)+(5*1)+(4*8)+(3*4)+(2*8)+(1*6)=83
83 % 10 = 3
So 2184-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11Cl2N/c1-2-3-8(7-14)10-5-4-9(12)6-11(10)13/h4-6,8H,2-3H2,1H3/t8-/m0/s1

2184-86-3SDS

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 2-(2,4-dichlorophenyl)pentanenitrile

1.2 Other means of identification

Product number -
Other names HMS1409M13

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:2184-86-3 SDS

2184-86-3Downstream Products

2184-86-3Relevant articles and documents

How iodide anions inhibit the phase-transfer catalyzed reactions of carbanions

Makosza, Mieczys?aw,Chesnokov, Alexey

, p. 5925 - 5932 (2008/12/20)

The inhibitory effect of iodide anions on the phase-transfer catalyzed reactions of carbanions generated in liquid-liquid two-phase systems by aqueous NaOH is due to preferential location of these anions in the interfacial region of the two-phase system-organic phase/concd aqueous NaOH. In such situation, the basic activity of NaOH in this region is decreased and the equilibrium of deprotonation of the carbanion precursors is disfavoured.

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