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3,3-Dimethyl-oxirane-2-carbonitrile, also known as 1,2-epoxy-3,3-dimethylcyclopropanecarbonitrile, is a chemical compound with the molecular formula C6H9NO. It is a colorless liquid with a molecular weight of 111.14 g/mol. 3,3-DIMETHYL-OXIRANE-2-CARBONITRILE is characterized by its epoxy and nitrile functional groups, which contribute to its reactivity and potential applications in various chemical processes. It is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain insecticides and herbicides. Due to its reactivity, it is important to handle 3,3-DIMETHYL-OXIRANE-2-CARBONITRILE with care, following appropriate safety protocols to minimize health and environmental risks.

6509-07-5

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6509-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6509-07-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6509-07:
(6*6)+(5*5)+(4*0)+(3*9)+(2*0)+(1*7)=95
95 % 10 = 5
So 6509-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO/c1-5(2)4(3-6)7-5/h4H,1-2H3

6509-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyloxirane-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 3,3-Dimethyl-oxirane-2-carbonitrile

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:6509-07-5 SDS

6509-07-5Relevant academic research and scientific papers

Expedient synthesis of glycidonitriles by darzens condensation of α-halogenonitriles with aldehydes and ketones

Jonczyk,Gadaj

, p. 1595 - 1610 (2008/09/17)

Chloroacetonitrile (1), α-halogenopropionitriles 4, and α-chlorophenylacetonitrile (6) react with aldehydes 2a,b,h-o and ketones 2c-g,p-t in the presence of solid NaOH in THF or DME, without any added catalyst, affording substituted glycidonitriles 3a-t, 5a, c-g,r,s and 7a,b,i,j,u,v, respectively (Darzens condensation). The glycidonitriles 3a-h, prepared from 1 and carbonyl compounds 2a-h, are obtained in high yields, exceeding those reported in the literature (Table 5). Expedient results of the reactions studied are due to increased reactivity of anions with Na+ as counterion in ethereal solvents. Investigation of the concentration of NaOH and the carbanion of diphenylacetonitrile in selected solvents reveals that ethereal solvents may increase the solubility of the anions participating in Darzens condensation.

Insertion of metallated epoxynitriles into organozirconocene chlorides. A convergent synthesis of 2-cyano-1,3-dienes

Kasatkin,Whitby

, p. 6201 - 6205 (2007/10/03)

Lithiated epoxynitriles insert efficiently into alkenyizirconocene chlorides via a 1,2-metallate rearrangement to form intermediates which eliminate Cp2Zr(Cl)O- to afford substituted 2-cyano-1,3-dienes. (C) 2000 Elsevier Science Ltd.

NOUVELLE VOIE DE SYNTHESE D'ACIDES AMINES MONOFLUORES

Ayi, A. I.,Remli, M.,Guedj, R.

, p. 1505 - 1508 (2007/10/02)

Ring opening of the glycidonitriles (IIa-e) by HF/pyridine leads to the fluorocyanohydrins (IIIa-e).Treatment of the nitriles (IIIa-e) with ammonia in methanol gives the α-amino-β-fluoro nitriles (IVa-e) which upon acidic hydrolysis afford the β-fluoro-α-

Two-phase Darzens Condensation Reaction with Octopus Compounds as a Catalyst

Akabori, Sadatoshi,Ohtomi, Michiko,Yatabe, Seiichi

, p. 1463 - 1464 (2007/10/02)

The octopus compound, readily derived from hexakis(mercaptomethyl)benzene and 1-chloro-3,6,9-triozadecane, was effectively employed as a catalyst in the two-phase Darzens condensation of carbonyl compounds with chloroacetonitrile to afford the correspondi

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