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Cycloheptylacetonitrile is a chemical compound with the molecular formula C9H15N. It is a cyclic compound consisting of a seven-membered ring (heptyl) attached to an acetonitrile group. cycloheptylacetonitrile is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Cycloheptylacetonitrile is known for its unique chemical properties, such as its reactivity towards nucleophilic addition and its ability to undergo electrophilic substitution reactions. It is typically synthesized through various methods, including the reaction of cycloheptanone with hydrocyanic acid or the addition of cyanide to cycloheptene. Due to its potential applications in the production of various chemicals and its role as a building block in organic synthesis, cycloheptylacetonitrile is a significant compound in the field of chemistry.

5452-65-3

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5452-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5452-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5452-65:
(6*5)+(5*4)+(4*5)+(3*2)+(2*6)+(1*5)=93
93 % 10 = 3
So 5452-65-3 is a valid CAS Registry Number.

5452-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cycloheptylacetonitrile

1.2 Other means of identification

Product number -
Other names Cycloheptaneacetonitrile

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:5452-65-3 SDS

5452-65-3Downstream Products

5452-65-3Relevant academic research and scientific papers

Photoinduced 1,2-Hydro(cyanomethylation) of Alkenes with a Cyanomethylphosphonium Ylide

Miura, Tomoya,Moriyama, Daisuke,Funakoshi, Yuuta,Murakami, Masahiro

supporting information, p. 511 - 514 (2019/02/26)

An efficient method has been developed for the 1,2-hydro(cyanomethylation) of alkenes, in which a cyanomethyl radical species is generated from a cyanomethylphosphonium ylide by irradiation with visible light in the presence of an iridium complex, a thiol, and ascorbic acid. The cyanomethyl radical species then adds across the C=C double bond of an alkene to form an elongated alkyl radical species that accepts a hydrogen atom from the thiol to produce an elongated aliphatic nitrile. The ascorbic acid acts as the reductant to complete the catalytic cycle.

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