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28269-82-1

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28269-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28269-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,6 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28269-82:
(7*2)+(6*8)+(5*2)+(4*6)+(3*9)+(2*8)+(1*2)=141
141 % 10 = 1
So 28269-82-1 is a valid CAS Registry Number.

28269-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N'-phenylcarbamimidothioate

1.2 Other means of identification

Product number -
Other names 1-phenyl-S-benzyl isothiocarbamide

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:28269-82-1 SDS

28269-82-1Relevant articles and documents

Synthesis and characterization of isothiobiurets of N-glucosylated compounds and their antimicrobial activities

Sarap, Ashish G.,Deshmukh, Shirish P.

, p. 1015 - 1018 (2013/09/23)

A series of several 1-aryl-5-tetra-O-acetyl-β-glucopyranosyl-2-S- benzyl-2-isothiobiurets have been prepared by the interaction of aryl S-benzylisothiocarbamides and tetra-O-acetyl-β-glucopyranosyl isocyanate. The required aryl S-benzylisothiocarbamides was prepared by S-benzylation of different thioureas and tetra-O-acetyl-β-D-glucopyranosyl isocyanate was prepared by interaction of tetra-O-acetyl-α-D-glucopyranosyl bromide and lead cyanate. The structures of the newly synthesized compounds have been established on the basis of usual chemical transformations and IR, 1H NMR and Mass spectral studies. All the synthesized compounds have been evaluated for their in vitro antibacterial and antifungal activity against different bacteria and fungi by agar diffusion method.

Synthesis of N-galactosylated isodithiobiurets

Mahalle, Prashant R.,Deshmukh, Shirish P.

experimental part, p. 742 - 745 (2009/12/05)

Several 1-aryl-5-tetra-O-acetyl-β-D-galactosyl-2-S-benzyl-2,4- isodithiobiurets have been prepared by the interaction of aryl-S-benzyl isothiocarbamides and tetra-O-acetyl-β-D-galactosyl isothiocyanate. The structures of the newly synthesized compounds have been established on the basis of usual chemical transformations and IR, NMR and Mass spectral studies.

2-Imidazolines. IV (1). 1-Aryl-2-alkylthio-4,5-diamino-4,5-dihydroimidazoles. Synthesis and Properties

Meola, Stefania,Rivera, Elisabetta,Stradi, Riccardo,Gioia, Bruno

, p. 1041 - 1044 (2007/10/02)

1,2-Diimmonium salts (1) react with S-substituted isothioureas (3) yielding 2-alkylthio-4,5-diamino-4,5-dihydroimidazoles (4), which under mild pyrolytic conditions afforded 2-alkylthio-5-aminoimidazoles (7).Imidazolines (4) and imidazoles (7) were easily

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