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3-(2-chlorophenyl)-2-cyanooxirane-2-carboxamide is a complex organic chemical compound with the molecular formula C10H6ClNO3. It is characterized by a 2-chlorophenyl group attached to a three-membered oxirane ring, which is further connected to a cyano group and a carboxamide functional group. 3-(2-chlorophenyl)-2-cyanooxirane-2-carboxamide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides. Its chemical structure and properties make it a versatile building block in organic synthesis, although it is important to handle it with care due to its potential reactivity and toxicity.

3513-09-5

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3513-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3513-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3513-09:
(6*3)+(5*5)+(4*1)+(3*3)+(2*0)+(1*9)=65
65 % 10 = 5
So 3513-09-5 is a valid CAS Registry Number.

3513-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-chlorophenyl)-2-cyanooxirane-2-carboxamide

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

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More Details:3513-09-5 SDS

3513-09-5Downstream Products

3513-09-5Relevant academic research and scientific papers

A NOVEL REARRANGEMENT OF THE ADDUCT FROM CS-EPOXIDE AND DIOXAN-2-HYDROPEROXIDE

Harrison, John M.,Inch, Thomas D.

, p. 679 - 682 (2007/10/02)

Under mild conditions, nucleophiles add across the cyanide moiety of CS epoxide rather than opening the ring.With hydroxide ion in peroxide-free aqueous dioxan isomeric amides are obtained.Hydrolysis in peroxide containing dioxan affords a novel rearrangement involving carbon-carbon bond fission of the dioxan.

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