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61784-88-1

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61784-88-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61784-88-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,8 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61784-88:
(7*6)+(6*1)+(5*7)+(4*8)+(3*4)+(2*8)+(1*8)=151
151 % 10 = 1
So 61784-88-1 is a valid CAS Registry Number.

61784-88-1SDS

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 1-ethyl-3-(phenylcarbamothioylamino)thiourea

1.2 Other means of identification

Product number -
Other names 1,2-Hydrazinedicarbothioamide,N-ethyl-N'-phenyl

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:61784-88-1 SDS

61784-88-1Relevant articles and documents

New condensed nitrogen–phosphorus heterocycles

?ev?ík, Richard,P?íhoda, Ji?í,Ne?as, Marek

, p. 96 - 103 (2017)

To extend our previous study aimed at the reactions of chlorodithiophosphoric acid pyridiniumbetaine (py·PS2Cl) with thiosemicarbazide derivatives, we performed the reactions of chlorodithiophosphoric acid pyridiniumbetaine with a new group of polyfunctional nucleophiles – symmetrical and nonsymmetrical derivatives of hydrazine-1,2-bis(thiocarboamide) of general formula R(H)N–C(S)N(H)N(H)C(S)–N(H)R (R?=?methyl, i-propyl, ethyl, t-butyl, phenyl). In analogy to heterocyclic anions obtained with the thiosemicarbazide derivatives, the hydrazine derivatives were expected to form heterobicyclic dianions from the reactions with py·PS2Cl. All the reactions were carried out in acetonitrile in the presence of pyridine to keep the same reaction conditions as with the previous experiments. Four new compounds were prepared and characterized by31P NMR, FTIR, Raman spectroscopy, and single crystal X-ray diffraction. Molecular structures of the products are based on heterobicyclic dianion consisting of two condensed five membered P–N–N–C–N rings, each of them bearing an organic group. Both of the organic groups in heterobicyclic dianion are either identical (Me,iPr) or different (Et/tBu, Et/Ph). The molecular structure of the heterobicyclic dianion with unusual structural features was further examined by quantum chemistry calculations.

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