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3,3-disulfanyl-1-(thiophen-2-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15185-52-1

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15185-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15185-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15185-52:
(7*1)+(6*5)+(5*1)+(4*8)+(3*5)+(2*5)+(1*2)=101
101 % 10 = 1
So 15185-52-1 is a valid CAS Registry Number.

15185-52-1SDS

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 3,3-bis(sulfanyl)-1-thiophen-2-ylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-oxo-3-thiophen-2-yl-dithiopropionic acid

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:15185-52-1 SDS

15185-52-1Relevant academic research and scientific papers

Oxoketene Dithiols: Synthesis of Some Heterocycles as Antimicrobials Utilizing Shrimp Chitin as a Natural Catalyst

Zayed, Salem E.,El-Maghraby, Awatef M.,Hassan, Entesar A.

, p. 1682 - 1698 (2015/10/29)

1, 2-dithiol 3-thione derivatives, as starting materials, were subjected to cycloaddition reactions in the presence of the dried outer shell of shrimp (chitin), under different reaction conditions to produce the 1, 3-dithiole-2-ylidene system. On treating 4-bromo dithiol 3-one, with dimethyl ester of acetylene dicarboxylic acid the bromo oxothiafulvene was produced. Further addition of DMAD to bromotrithiafulvene afforded the spiro bromo derivative. Trithiones and trithiafulvenes were also added to quinones, cyclohexadiene and cyclopentadiene monomer, and the corresponding adducts were produced through 1,3-dipole cycloaddition reactions. On testing some of the products against the isolated micro-organisms from sugar cane factory, the inhibition zones at concentration 1 × 10-6 were found. Products (2, 6, 9, 16, 23, 25, and 26) showed high activities against Bacillus sub., E.Coli and Asper. Niger.

Thiafulvenes and thiafulvalenes in organic chemistry: Synthesis and study its behavior towards some chemical reagents

Zayed, Salem E.,Hassan, M. Ezel-Dean,Ragab, Rawia

, p. 2205 - 2216 (2008/02/10)

Trithiafulvenes were prepared through cycloaddition of 3-thioxo-1,2- dithioles to several electrophilic alkenes and alkynes. Treatments of the product with phenyl-hydrazine and malononitrile afforded the hydrazone and the dinitrilene derivatives respectiv

Ketoken gem-dithiols and trithiones: Synthesis and study of the behavior towards dipole reagents; Synthesis of some nitrogen heteroaromatics

Zayed, Salem E.

, p. 7 - 13 (2007/10/03)

The behavior of ketoken gem-dithiols towards active methylene and methyl groups resulted in the formation of thiopyrano-dihydrocaumarine derivatives IIIa,b via cyclocondensation reaction between substituted 4-dihydrocyclohexanone Ia.b. N-phenylpyrazoline

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