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70466-79-4

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70466-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70466-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70466-79:
(7*7)+(6*0)+(5*4)+(4*6)+(3*6)+(2*7)+(1*9)=134
134 % 10 = 4
So 70466-79-4 is a valid CAS Registry Number.

70466-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-3-(sulfamoylamino)benzene

1.2 Other means of identification

Product number -
Other names N-(3-nitrophenyl)sulfamide

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:70466-79-4 SDS

70466-79-4Upstream product

70466-79-4Downstream Products

70466-79-4Relevant articles and documents

Basicity of Nitrogen-Sulphur(VI) Compounds. Part 6. Ionization of NN'-Di- and N-Mono-substituted Sulphamides and Dihydro-2,1,3-benzothiadiazoline and Benzothiadiazine 2,2-Dioxides (Cyclic Sulphamides)

Burke, Padraig O.,McDermott, Sean D.,Hannigan, Thomas J.,Spillane, William J.

, p. 1851 - 1854 (2007/10/02)

36 Di- and mono- and two tri-substituted sulphamides have been synthesised and their ionization equilibria in base (Schemes 1-3) have been studied.Many of the sulphamides are new materials.The pKa values obtained for each series have been correlated in Hammett and Taft plots.The Hammett ? values obtained for the ionization of the proximate hydrogen are ca. 2.3.The Taft ?* value obtained for ionization of the 'remoter' hydrogen is 1.68.The six-membered cyclic sulphamides are more acidic than their acyclic analogues by ca. 2.5 pKa units and the five-membered cyclic sulphamides are ca. 4 pKa units more acidic than model open-chain counterparts.Sulphur d-orbital involvement and ring-strain are suggested as possible sources of this 'acid-strengthening' effect.

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