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187587-70-8

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187587-70-8 Usage

Description

4-(Methylsulfinyl)-1-butylamine, with the chemical formula C5H13NO2S, is an organic compound characterized by a yellow liquid appearance. It is known for its unique chemical properties and is utilized in various organic synthesis processes.

Uses

Used in Organic Synthesis:
4-(Methylsulfinyl)-1-butylamine is used as a synthetic intermediate for the production of various organic compounds. Its presence in the synthesis process aids in the formation of complex organic molecules, which can be further utilized in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-(Methylsulfinyl)-1-butylamine is used as a building block for the development of new drugs. Its unique structure allows it to be incorporated into the molecular design of potential therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
4-(Methylsulfinyl)-1-butylamine is also employed in chemical research as a reagent or a precursor in various chemical reactions. It helps researchers explore new reaction pathways and develop innovative synthetic methods.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(Methylsulfinyl)-1-butylamine is used as a component in the synthesis of pesticides and other agrochemicals. Its role in these processes is crucial for the development of effective and environmentally friendly products.
Used in Flavor and Fragrance Industry:
4-(Methylsulfinyl)-1-butylamine is utilized in the flavor and fragrance industry as a precursor for the creation of unique scents and flavors. Its chemical properties allow it to be transformed into a variety of aromatic compounds, enhancing the sensory experience of various products.

Check Digit Verification of cas no

The CAS Registry Mumber 187587-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,5,8 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 187587-70:
(8*1)+(7*8)+(6*7)+(5*5)+(4*8)+(3*7)+(2*7)+(1*0)=198
198 % 10 = 8
So 187587-70-8 is a valid CAS Registry Number.

187587-70-8SDS

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 4-(Methylsulfinyl)-1-butanamine

1.2 Other means of identification

Product number -
Other names -

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:187587-70-8 SDS

187587-70-8Relevant articles and documents

A facile and efficient synthesis of 14C-labelled sulforaphane

D'Souza, Christopher A.,Amin, Shantu,Desai, Dhimant

, p. 851 - 859 (2003)

Isothiocyanates have gained considerable attention for their role as potent chemopreventive agents. Sulforaphane, 1a (SFN), a naturally occurring isothiocyanate, was isotopically labelled in five steps starting from 3-(methylthio)-1-propanol (2). Reacting 2 with tosyl chloride in the presence of Et3N yielded the tosylate 3. Gently refluxing 3 with K 14CN in DMF gave the nitrile 4b. Reduction to the amine 5b was achieved using BH3-THF. Oxidation with 30% hydrogen peroxide followed by treatment with thiophosgene yielded (±)[1-14C]SFN, 1b. The overall radiochemical yield was 4.4% based on the starting K 14CN. Copyright

PROCESS FOR THE SYNTHESIS OF ISOTHIOCYANATES AND DERIVATIVES THEREOF AND USES OF SAME

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Paragraph 0111-0128, (2013/06/26)

A method for synthesizing an isothiocyanate of general formula (I) [in-line-formulae]SCN—R1—R4—R2??(I)[/in-line-formulae] wherein R1 and R2 represent independently of each other an alkyl-aryl or aryl group, R4 represents a carbonyl, sulfinyl, sulfonyl group or a sulfide group and of its derivatives comprising a step for reacting an alkylalkylamine having the general formula (II) [in-line-formulae]NH2—R1—R4—R2??(II)[/in-line-formulae] wherein R1 and R2 represent independently of each other an alkyl, aryl or alkylaryl group, R4 represents a carbonyl, sulfinyl, sulfonyl or sulfide group, in the presence of carbon sulfide and of di-tert-butyl dicarbonate with formation of the corresponding aforesaid isothiocyanate, compounds obtained by this method as well as their uses.

Stabilized sulforaphane

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Page/Page column 8, (2008/12/07)

A method of stabilizing sulforaphane is provided. The method includes contacting sulforaphane, or an analog thereof, and a cyclodextrin to form a complex between the sulforaphane, or analog thereof, and the cyclodextrin.

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