Welcome to LookChem.com Sign In|Join Free
  • or
N-(BUTYLTHIO)ACETONITRILE, with the molecular formula C6H11NS, is a colorless liquid characterized by a pungent odor. It is a versatile chemical compound that serves as a crucial intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its ability to form carbon-sulfur bonds makes it particularly valuable in organic chemistry reactions.

71037-08-6

Post Buying Request

71037-08-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

71037-08-6 Usage

Uses

Used in Pharmaceutical Industry:
N-(BUTYLTHIO)ACETONITRILE is used as a synthetic intermediate for the production of various pharmaceuticals. Its role in creating carbon-sulfur bonds is essential in the synthesis of a range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, N-(BUTYLTHIO)ACETONITRILE is utilized as a precursor in the synthesis of agrochemicals. Its involvement in the formation of specific chemical bonds is vital for the creation of effective pesticides and other agricultural chemicals that protect crops and enhance yields.
Used in Organic Chemistry Research:
N-(BUTYLTHIO)ACETONITRILE is employed as a reagent in organic chemistry research. Its capacity to form carbon-sulfur bonds is instrumental in advancing the understanding of chemical reactions and the development of novel organic compounds for various applications.
Safety Precautions:
Given its harmful nature if swallowed or absorbed through the skin, it is imperative to exercise appropriate safety measures when handling N-(BUTYLTHIO)ACETONITRILE. This includes the use of personal protective equipment and adherence to safety protocols to minimize exposure and potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 71037-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,3 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71037-08:
(7*7)+(6*1)+(5*0)+(4*3)+(3*7)+(2*0)+(1*8)=96
96 % 10 = 6
So 71037-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NS/c1-2-3-5-8-6-4-7/h2-3,5-6H2,1H3

71037-08-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B22336)  n-(Butylthio)acetonitrile, 95%   

  • 71037-08-6

  • 5g

  • 240.0CNY

  • Detail
  • Alfa Aesar

  • (B22336)  n-(Butylthio)acetonitrile, 95%   

  • 71037-08-6

  • 25g

  • 1037.0CNY

  • Detail

71037-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butylsulfanylacetonitrile

1.2 Other means of identification

Product number -
Other names 1-Butyl cyanomethyl sulfide

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:71037-08-6 SDS

71037-08-6Relevant academic research and scientific papers

Electrochemical Alkylation of Thiols

Petrosyan, V. A.,Niyazymbetov, M. E.,Konyushkin, L. D.,Litvinov, V. P.

, p. 841 - 842 (2007/10/02)

Synthesis of functionally substituted sulfides by alkylation of electrochemically generated thiolate on platinum or glassy carbon cathodes with organohalides of various structures is reported.

ELECTROCHEMICAL SYNTHESIS OF FUNCTIONALLY SUBSTITUTED SULFIDES

Niyazymbetov, M. E.,Petrosyan, V. A.,Konyushkin, L. D.,Litvinov, V. P.

, p. 1454 - 1457 (2007/10/02)

A method of synthesis of functionally substituted sulfides by cathode electrolysis of thiols on platinum or carbon glass electrodes in the presence of organyl halides was developed.The method of the rotating disk electrode with ring showed that this process passes through the intermediate formation of a thiolate anion on the cathode, and its reaction with the organyl halide results in a high yield of sulfides.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 71037-08-6