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18967-42-5

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18967-42-5 Usage

General Description

3,4-Dichlorobenzyl isothiocyanate is a synthetic organosulfur compound with potential applications in both medical and industrial contexts. It contains both chlorine and sulfur groups, with the former known for its disinfectant properties and the latter often used in the production of rubber and other polymers. 3,4-DICHLOROBENZYL ISOTHIOCYANATE may also have utility in pharmaceuticals due to isothiocyanates being known for their anti-carcinogenic, anti-inflammatory, and immune-modulating properties. However, due to its potentially harmful effects, the use of 3,4-dichlorobenzyl isothiocyanate must be thoroughly tested and regulated.

Check Digit Verification of cas no

The CAS Registry Mumber 18967-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,6 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18967-42:
(7*1)+(6*8)+(5*9)+(4*6)+(3*7)+(2*4)+(1*2)=155
155 % 10 = 5
So 18967-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NS/c9-7-2-1-6(3-8(7)10)4-11-5-12/h1-3H,4H2

18967-42-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L11701)  3,4-Dichlorobenzyl isothiocyanate, 97%   

  • 18967-42-5

  • 1g

  • 415.0CNY

  • Detail
  • Alfa Aesar

  • (L11701)  3,4-Dichlorobenzyl isothiocyanate, 97%   

  • 18967-42-5

  • 5g

  • 1603.0CNY

  • Detail

18967-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dichloro-4-(isothiocyanatomethyl)benzene

1.2 Other means of identification

Product number -
Other names 3,4-Dichlorobenzyl isothiocyanate

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:18967-42-5 SDS

18967-42-5Relevant articles and documents

Synthesis and Octopaminergic Agonist Activity of 2-(Substituted benzylamino)-2-thiazolines

Hirashima, Akinori,Yoshii, Yutaka,Eto, Morifusa

, p. 1062 - 1065 (2007/10/02)

2-(Substituted benzylamino)-2-thiazolines (SBAT) were synthesized by a hydrochloric acid-catalyzed cyclization of the corresponding thioureas, using a reaction of 2-methylthio-2-thiazoline with substituted benzylamines or by alkylating 2-amino-2-thiazoline. 2-(Alkylthio)-2-thiazolines were obtained by alkylating 2-mercaptothiazoline.Most of the SBAT compounds activated adenylate cyclase in homogenates of cockroach ventral nerve cords; the effect of introducing substituents at the phenyl of the SBAT compounds on octopaminergic agonist activity was not significant. 2--2-thiazolines and 2-(alkylthio)-2-thiazolines were not significant octopaminergic agonists.Washing removed nearly all of the activity of one of the SBAT compounds, suggesting that the SBAT compounds bound reversibly to the octopaminergic receptor.

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