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Ethylenebis(isothiocyanate), also known as EBIS or ETU, is a chemical compound with the formula C4H6N2S2. It is a colorless to pale yellow liquid with a pungent odor and is used as a cross-linking agent in the production of polyurethane foams and elastomers. EBIS is also employed as a pesticide and a fungicide, particularly for the control of soil-borne diseases in agriculture. Due to its high reactivity and potential health risks, it is classified as a hazardous substance and requires careful handling and storage.

3688-08-2

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3688-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3688-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,8 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3688-08:
(6*3)+(5*6)+(4*8)+(3*8)+(2*0)+(1*8)=112
112 % 10 = 2
So 3688-08-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2S2/c7-3-5-1-2-6-4-8/h1-2H2

3688-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diisothiocyanatoethane

1.2 Other means of identification

Product number -
Other names Dimethylene diisothiocyanate

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:3688-08-2 SDS

3688-08-2Relevant academic research and scientific papers

Probing A-form DNA: A fluorescent aminosugar probe and dual recognition by anthraquinone-neomycin conjugates

Watkins, Derrick,Gong, Changjun,Kellish, Patrick,Arya, Dev P.

, p. 1309 - 1319 (2017)

Nucleic acids adopt a broad array of hydrogen-bonded structures that enable their diverse roles in the cell; even the familiar DNA double helix displays subtle architectural nuances that are sequence dependent. While there have been many approaches for recognition of B-form nucleic acids, A-form DNA recognition has lagged behind. Here, using a tight binding fluorescein-neomycin (F-neo) conjugate that can probe the electrostatic environment of A-form DNA major groove, we developed a fluorescent displacement assay to be used as a screen for DNA duplex-binding compounds. As opposed to intercalating dyes that can significantly perturb DNA structure, the groove binding F-neo allows the probing of native DNA conformation. In combination with the assay development and probing of DNA grooves, we also report the synthesis and binding of a series of neomycin-anthraquinone conjugates, two units with a known preference for binding GC rich DNA. The assay can be used to identify duplex DNA-binding compounds, as well as probe structural features of a target DNA duplex, and can easily be scaled up for high throughput screening of compound libraries.

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