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1115-06-6

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1115-06-6 Usage

Description

(dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane, also known as dimethylthioxamoyl dimethyldisulfide, is a thioxomethane derivative with the chemical formula C6H15NOS3. It is a white to off-white powder containing nitrogen, oxygen, sulfur, and carbon atoms, and has a molecular weight of 225.32 g/mol. (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is recognized for its unique chemical properties and is utilized as a reagent in organic synthesis.

Uses

Used in Pharmaceutical Industry:
(dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is used as a reagent for [application reason] in the pharmaceutical industry. Its unique chemical properties make it an important intermediate in chemical reactions, contributing to the development of various medications.
Used in Agrochemical Industry:
In the agrochemical industry, (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is used as a reagent for [application reason]. Its role in organic synthesis aids in the creation of compounds that can be applied in agriculture for pest control, crop protection, and other related purposes.
Used in Chemical Reactions:
As an important intermediate in chemical reactions, (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is used for [application reason]. Its presence in these reactions facilitates the synthesis of a range of compounds, which can be further utilized in various applications across different industries.
Used in Medicine:
(dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane has potential applications in the field of medicine due to its unique chemical properties. It is used as a [application type] for [application reason], potentially contributing to the development of new therapeutic agents or diagnostic tools.
Used in Agriculture:
In agriculture, (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is used as a [application type] for [application reason]. Its role in chemical reactions can lead to the creation of compounds that enhance crop yield, improve resistance to diseases, or provide other benefits to the agricultural sector.

Check Digit Verification of cas no

The CAS Registry Mumber 1115-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1115-06:
(6*1)+(5*1)+(4*1)+(3*5)+(2*0)+(1*6)=36
36 % 10 = 6
So 1115-06-6 is a valid CAS Registry Number.

1115-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name S-(dimethylcarbamothioylsulfanyl) N,N-dimethylcarbamothioate

1.2 Other means of identification

Product number -
Other names Dimethylcarbamoyl-dimethylthiocarbamoyl-disulfid

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:1115-06-6 SDS

1115-06-6Downstream Products

1115-06-6Relevant articles and documents

THE REACTION OF t-BUTYL HYPOCHLORITE WITH THIOCARBONYL COMPOUND - A CONVENIENT METHOD FOR THE TRANSFORMATION

El-Wassimy, M.T.M.,Jorgensen, K.A.,Lawesson, S.-O.

, p. 1729 - 1734 (2007/10/02)

The reaction of t-butyl hypochlorite with different thiocarbonyl compounds has been studied.Primary thioamides 1a-c give 1,2,4-thiadiazole derivatives.N-Phenylthiourea 4a gives 5-imino-4-phenyl-3-phenylamino-4,5-dihydro-1,2,4-thiadiazoline 15.Secondary and tertiary thioamides 2a-d, N-methyl-2-thiopyrrolidinone 3, N,N'-dicyclohexylthiourea 4b, N,N,N'-trimethylthiourea 4c, 5-ethyl-5-phenylthiobarbituric acid 5, xanthione 7a, Mischler's thioketone 7b, thiocoumarin 8, O-ethylthiobenzoate 9, O,O-diphenylthiocarbonate 10, di-p-tolyl and o-phenylene trithiocarbonates 11 and 12 have all afforded the oxigen analogues.N,N-Dimethyl-S-phenyldithiocarbonate 6 produces a mixture of di-, tri-, and tetrasulfides.A mechanism for the transformation is suggested in accordance with the Hard and Soft Acids and Bases (HSAB) principle.

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