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Carbamothioic acid, dimethyl-, S-(4-iodophenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84695-07-8

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84695-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84695-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84695-07:
(7*8)+(6*4)+(5*6)+(4*9)+(3*5)+(2*0)+(1*7)=168
168 % 10 = 8
So 84695-07-8 is a valid CAS Registry Number.

84695-07-8SDS

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 4-[(N,N'-Dimethylcarbamoyl)thio]iodobenzene

1.2 Other means of identification

Product number -
Other names S-4-iodophenyl N,N-dimethylthiocarbamate

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:84695-07-8 SDS

84695-07-8Relevant academic research and scientific papers

An improved synthesis and structural characterisation of 2-(4-acetylthiophenylethynyl)-4-nitro-5-phenylethynylaniline: The molecule showing high negative differential resistance (NDR)

Wang, Changsheng,Batsanov, Andrei S.,Bryce, Martin R.,Sage, Ian

, p. 2089 - 2095 (2007/10/03)

2-(4-Acetylthiophenylethynyl)-4-nitro-5-phenyl-ethynylaniline (11) has been synthesised by an improved route, which has many advantages over the literature procedure. A key intermediate is 2-ethynyl-4-nitro-5-phenylethynylaniline (6) which is obtained fro

Infrared Spectra and Transmission of Electronic Effects in Substituted Phenyl N,N-Dimethylcarbamates and S-Phenyl N,N-Dimethylthiocarbamates

Perjessy, Alexander,Jones, Ronald G.,McClair, Susan L.,Wilkins, Joyce M.

, p. 1266 - 1271 (2007/10/02)

Carbonyl stretching frequencies in CCl4 and CHCl3 and hydroxyl stretching frequency shifts of phenol as a proton donor in CCl4 were measured for series of substituted phenyl N,N-dimethylcarbamates (I) and S-phenyl N,N-dimethylthiocarbamates (II).The data

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