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67398-25-8

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67398-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67398-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67398-25:
(7*6)+(6*7)+(5*3)+(4*9)+(3*8)+(2*2)+(1*5)=168
168 % 10 = 8
So 67398-25-8 is a valid CAS Registry Number.

67398-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name O,O-diphenyl 1-(3-phenylthioureido)butanephosphonate

1.2 Other means of identification

Product number -
Other names [1-(3-phenyl-thioureido)-butyl]-phosphonic acid diphenyl ester

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:67398-25-8 SDS

67398-25-8Downstream Products

67398-25-8Relevant articles and documents

High-performance liquid chromatographic enantioseparation of N-aryl-thioureidoalkylphosphonates and thiourylenedi(alkylphosphonates) on polysaccharide-based chiral stationary phases

Drabowicz, Józef,Kudzin, Marcin H.,Kudzin, Zbigniew H.,Pokora-Sobczak, Patrycja

supporting information, p. 131 - 140 (2017/12/28)

The first successful enantioseparation of representative O,O-diphenyl-N-arylthioureidoalkylphosphonates, (±)-Ptc-ValP(OPh)2 & (±)-Ptc-LeuP(OPh)2 and thiourylenedi(isobutyl phosphonate), Tcm[ValP(OPh)2]2 on analytical and semipreparative scale was achieved by high-performance liquid chromatography using polysaccharide-based chiral stationary phases (CPs). Atc-AAP(OPh)2 was obtained using modified tricomponent condensations of the corresponding aldehydes, N-arylthiourea and triphenyl phosphite whereas Tcm[ValP(OPh)2]2 by the condensations of aldehydes, thiourea, and triphenyl phosphite. The prepared, racemic (±)-Atc-AAP(OPh)2 [(±)-Ptc-ValP(OPh)2, (±)-Ptc-LeuP(OPh)2, (±)-Ptc-PglyP(OPh)2 and (±)-Ntc-PglyP(OPh)2] and racemic (±)-Tcm[AAP(OPh)2]2 [(±)-Tcm[NvaP(OPh)2]2 & (±)-Tcm[ValP(OPh)2]2] were adequately characterized and used for chromatographic separations on high-performance liquid chromatography–chiral stationary phases. The best results were obtained for (±)-Ptc-ValP(OPh)2, (±)-Ptc-LeuP(OPh)2 and (±)-Tcm[ValP(OPh)2]2.

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