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61698-72-4

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61698-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61698-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,9 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61698-72:
(7*6)+(6*1)+(5*6)+(4*9)+(3*8)+(2*7)+(1*2)=154
154 % 10 = 4
So 61698-72-4 is a valid CAS Registry Number.

61698-72-4SDS

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 2-phenylsulfanyl-N,N-di(propan-2-yl)acetamide

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:61698-72-4 SDS

61698-72-4Relevant articles and documents

Extraction and coordination studies of the unexplored bifunctional ligand carbamoyl methyl sulfoxide (CMSO) with uranium(VI) and cerium(III) nitrates. Synthesis and structures of [UO2(NO3) 2(PhSOCH2CONi

Kannan, Shanmugaperumal,Chetty, Kuna Venugopal,Venugopal, Venkatarama,Drew, Michael G. B.

, p. 3604 - 3610 (2004)

The bifunctional carbamoyl methyl sulfoxide ligands, PhCH 2SOCH2CONHPh (L1), PhCH2SOCH 2CONHCH2Ph (L2), PhSOCH2CON iPr2 (L3), PhSOCHs

Facile syntheses of 2,2-dimethyl-6-(2-oxoalkyl)-1,3-dioxin-4-ones and the corresponding 6-substituted 4-hydroxy-2-pyrones

Katritzky, Alan R.,Wang, Zuoquan,Wang, Mingyi,Hall, C. Dennis,Suzuki, Kazuyuki

, p. 4854 - 4856 (2007/10/03)

A variety of 2,2-dimethyl-6-(2-oxoalkyl)-1,3-dioxin-4-ones 5a-l and the corresponding 6-substituted 4-hydroxy-2-pyrones 3a-l were prepared in high yields under mild reaction conditions by the reaction of 2,2,6-trimethyl-1,3- dioxin-4-one 4 with 1-acylbenz

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