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Benzonitrile, 4-(5-ethyl-1,3-dithian-2-yl)-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92974-20-4

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92974-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92974-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,7 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92974-20:
(7*9)+(6*2)+(5*9)+(4*7)+(3*4)+(2*2)+(1*0)=164
164 % 10 = 4
So 92974-20-4 is a valid CAS Registry Number.

92974-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Ethyl-[1,3]dithian-2-yl)-benzonitrile

1.2 Other means of identification

Product number -
Other names -

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:92974-20-4 SDS

92974-20-4Downstream Products

92974-20-4Relevant academic research and scientific papers

LIQUID CRYSTAL MATERIALS WITH SULFUR ATOMS INCORPORATED IN THE PRINCIPAL STRUCTURE: 1. NEW LIQUID CRYSTAL COMPOUNDS WITH 1,3-DITHIANE RING.

Haramoto,Nobe,Kamogawa

, p. 1966 - 1969 (2007/10/02)

2-(p-Substituted phenyl)-5-alkyl-1,3-dithianes, new liquid crystals, were synthesized by the thioacetalization of the corresponding aldehydes and dithiols. These compounds have characteristic supercooling states, exhibit monotropic liquid crystal phases even in the case of long terminal alkyl substituents. The mesomorphic characteristics of these compounds were different from those of the corresponding 1,3-dioxanes, this must originate in the difference in the molecular width caused by the difference in the atomic volume between sulfur and oxygen.

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