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3,4-Epithiobutanenitrile, also known as 3,4-epithiobutyronitrile, is a chemical compound with the formula C4H7NS. It is a colorless liquid with a pungent odor and is recognized for its role as an intermediate in the synthesis of various products, particularly in the pharmaceutical and agrochemical industries. Its utility extends to the creation of other organic compounds, such as those used in dyes, flavors, and fragrances. Due to its high toxicity, it requires careful handling to prevent skin, eye, and respiratory irritation, as well as potential damage to the central nervous system and organs from prolonged or high-level exposure.

58130-93-1

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58130-93-1 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Epithiobutanenitrile is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and therapeutic agents. Its chemical properties make it a valuable building block in the creation of complex organic molecules with potential medicinal applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3,4-Epithiobutanenitrile serves as an essential intermediate in the production of various agrochemicals, including pesticides and herbicides. Its role in these applications is crucial for enhancing crop protection and increasing agricultural productivity.
Used in Dye, Flavor, and Fragrance Industries:
3,4-Epithiobutanenitrile is utilized as a building block in the manufacturing of dyes, flavors, and fragrances, where its unique chemical structure contributes to the creation of a wide range of colorants, taste modifiers, and scent compounds for various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 58130-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58130-93:
(7*5)+(6*8)+(5*1)+(4*3)+(3*0)+(2*9)+(1*3)=121
121 % 10 = 1
So 58130-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H5NS/c5-2-1-4-3-6-4/h4H,1,3H2

58130-93-1SDS

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 2-(thiiran-2-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names Thiiraneacetonitrile

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:58130-93-1 SDS

58130-93-1Upstream product

58130-93-1Downstream Products

58130-93-1Relevant academic research and scientific papers

INTERACTIONS OF THIOGLUCOSIDE GLUCOHYDROLASE AND EPITHIOSPECIFIER PROTEIN OF CRUCIFEROUS PLANTS TO FORM 1-CYANOEPITHIOALKANES

Petroski, Richard J.,Tookey, Harvey L.

, p. 1903 - 1906 (1982)

Allylglucosinolate is converted to 1-cyano-2,3-epithiopropane by interaction of the thioglucoside glucohydrolase and epithiospecifier protein from several genera: Brassica, Crambe, Armoracia and Sinapis.The interactions occur across genetic lines, indicating non-specific requirements for epithiospecifier protein and thioglucoside glucohydrolase.Key Word Index - Cruciferae; thioglucoside glucohydrolase; thioglucosidase; epithiospecifier protein; glucosinolate; 1-cyanoepithioalkanes; 1-cyano-2,3-epithiopropane.

INTERACTIONS OF A FUNGAL THIOGLUCOSIDE GLUCOHYDROLASE AND CRUCIFEROUS PLANT EPITHIOSPECIFIER PROTEIN TO FORM 1-CYANOEPITHIOALKANES: IMPLICATIONS OF AN ALLOSTERIC MECHANISM

Petroski, Richard J.,Kwolek, William F.

, p. 213 - 216 (2007/10/02)

Allylglucosinolate is converted to 1-cyano-2,3-epithiopropane by interaction of the thioglucoside glucohydrolase from the fungus Aspergillus sydowi QM 31c and the epithiospecifier protein from Crambe abyssinica.The kinetic evidence presented supports the hypothesis that the epithiospecifier protein interacts with thioglucoside glucohydrolase in allosteric manner.Key Word Index - Crambe abyssinica; Cruciferae; Aspergillus sydowi; thioglucoside glucohydrolase; thioglucosidase; epithiospecifier protein; crucifer; glucosinolate; 1-cyanoepithioalkanes; 1-cyano-2,3-epithiopropane.

THE INTRAMOLECULAR FORMATION OF EPITHIOALKANENITRILES FROM ALKENYLGLUCOSINOLATES BY CRAMBE ABYSSINICA SED FLOUR

Brocker, Erich R.,Benn, M. H.

, p. 770 - 772 (2007/10/02)

Enzymatic degradations of mixtures of potassium 3-butenylglucosinolate and allylglucosinolate by aqueous suspensions of Crambe abyssinica seed flour led to the formation of 4,5-epithiopentanenitrile and essentially unlabelled 3,4-epithiobutanenitrile.The formation of epithioalkanenitriles from alkenylglucosinolates is, therefore deduced to be an intramolecular process. -- Key Word Index - Crambe abyssinica; Cruciferae; allylglucosinolate; 3-butenylglucosinolate; 3,4-epithiobutanenitrile; 4,5-epithiopentanenitrile; sinigrin; episulphide; thiirane; biosynthesis.

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