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ethyl cyano(9H-xanthen-9-ylidene)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65714-65-0

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65714-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65714-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,1 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65714-65:
(7*6)+(6*5)+(5*7)+(4*1)+(3*4)+(2*6)+(1*5)=140
140 % 10 = 0
So 65714-65-0 is a valid CAS Registry Number.

65714-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-cyano-2-xanthen-9-ylideneacetate

1.2 Other means of identification

Product number -
Other names cyano-xanthen-9-ylidene-acetic acid ethyl ester

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:65714-65-0 SDS

65714-65-0Downstream Products

65714-65-0Relevant academic research and scientific papers

Reactions of 4-Chloro-9H-xanthene-9-thione with Tetrachloro-o-benzoquinone

Zeid, Ibrahim,El-Sakka, Ibrahim,Yassin, Salah,Abass, Atif

, p. 196 - 198 (2007/10/02)

Thiones are usually converted to the corresponding ketones by oxidizing agents.Also high potential halogenated o-quinones oxidize thiones to the corresponding ketones.When 9H-thioxanthene-9-thione was subjected to the action of tetrachloro-o-benzoquinone the in presence of oxygen, it was oxidized to 9H-thioxanthen-9-one.Meanwhile tetrachloro- and tetrabromo-o-benzoquinones were found to react with diazoalkanes giving the corresponding cyclic acetals.

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