Welcome to LookChem.com Sign In|Join Free

CAS

  • or

111039-41-9

Post Buying Request

111039-41-9 Suppliers

Recommended suppliersmore

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

111039-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111039-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,3 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111039-41:
(8*1)+(7*1)+(6*1)+(5*0)+(4*3)+(3*9)+(2*4)+(1*1)=69
69 % 10 = 9
So 111039-41-9 is a valid CAS Registry Number.

111039-41-9SDS

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-(4-bromobenzyl)isothiourea hydrobromide

1.2 Other means of identification

Product number -
Other names .S-(4-bromo-benzyl)-isothiourea, hydrobromide

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:111039-41-9 SDS

111039-41-9Relevant articles and documents

Synthesis of difluoromethyl and deuterium-labeled difluoromethyl thioethers from aliphatic electrophiles

Ding, Tianqi,Jiang, Lvqi,Yi, Wenbin

, p. 3995 - 3998 (2020/04/17)

A one-pot difluoromethylthiolation of alkyl electrophiles with thiourea and diethyl bromodifluoromethylphosphonate is described. The transition-metal-free approach, readily available reagents, and mild conditions provide a practical way for the synthesis of difluoromethyl thioethers. By changing the "H" source to the most commonly used "D" sources CD3OD and D2O, this strategy enables efficient synthesis of SCF2D-substituted molecules in good yields with high levels of D incorporation.

Synthesis of 2-(Benzylthio)-4-(trifluoromethyl)thiazole-5-carboxylates Using S -Benzylisothiouronium Halides as Thiol Equivalents

Hickey, Shane M.,White, Jonathan M.,Pfeffer, Frederick M.,Ashton, Trent D.

supporting information, p. 1759 - 1763 (2015/07/20)

S-Benzylisothiouronium halides are used as shelf-stable, odorless thiol equivalents. The method developed is used to access 2-(benzylthio)-4-(trifluoromethyl)thiazole carboxyl building blocks. Using the latent trifluoromethyl substituent the reactions could be monitored using 19F NMR spectroscopy.

Synthesis and antimicrobial and nitric oxide synthase inhibitory activities of novel isothiourea derivatives

Kazimierczuk, Zygmunt,Chalimoniuk, Malgorzata,Laudy, Agnieszka Ewa,Moo-Puc, Rosa,Cedillo-Rivera, Roberto,Starosciak, Bohdan Jerzy,Chrapusta, Stanislaw J.

experimental part, p. 821 - 830 (2012/01/05)

The reaction of substituted benzylhalides, or of halomethyl derivatives of thiophene or furane, with thiourea or its derivatives yielded the respective isothioureas as hydrohalide salts. The products (a total of 17, including 16 novel compounds) were test

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

What can I do for you?
Get Best Price

Get Best Price for 111039-41-9