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19822-35-6

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19822-35-6 Usage

General Description

4-Isothiocyanato-4'-Nitrodiphenyl Sulfide is a chemical compound known for its unique structure and properties. As an organic compound, it contains isothiocyanato and nitro functional groups, contributing to its chemical behaviour and reactivity. It is a result of a specific chemical synthesis process, often involving the transformation of chemical functionalities through specific reactions. The structure of the compound signifies the presence of sulfur and nitrogen, which play key roles in its interactions and properties. Its detailed characteristics, such as melting/boiling point, density, molecular weight, or possible applications, can depend on the exact conditions and experimental methods used during its characterization. It's mainly used in scientific research as a synthesizing agent.

Check Digit Verification of cas no

The CAS Registry Mumber 19822-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19822-35:
(7*1)+(6*9)+(5*8)+(4*2)+(3*2)+(2*3)+(1*5)=126
126 % 10 = 6
So 19822-35-6 is a valid CAS Registry Number.

19822-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Isothiocyanato-4'-nitrodiphenyl sulfide

1.2 Other means of identification

Product number -
Other names 1-isothiocyanato-4-(4-nitrophenyl)sulfanylbenzene

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:19822-35-6 SDS

19822-35-6Relevant articles and documents

Design, synthesis and bioactivities of phenithionate analogues or derivatives for anti-schistosomiasis

Zhou, Shiyang,Huang, Gangliang

, p. 328 - 336 (2018/03/08)

A novel series of phenithionate analogues or derivatives were designed and synthesized using phenithionate as the lead compound, and their bioactivities were studied. Their structures were confirmed by 1H NMR, 13C NMR, HR-ESI-MS, and elemental analysis, respectively. The results of in vitro inhibitory activity measurement proved that compounds 5a, 5c, 5g, 5i, 5m and 5o had a better inhibitory effect on larva and imago schistosoma. Among them, the inhibitory activity of compound 5i for larva schistosoma was IC50 = 5.21 ± 0.04 μg mL-1, and for imago schistosoma it was IC50 = 6.35 ± 0.08 μg mL-1. Moreover, the experimental results of in vivo anti-schistosomiasis activity measurement showed that they had good anti-schistosomiasis activity. Therefore, these compounds had better drugability.

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