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13195-52-3

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13195-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13195-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,9 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13195-52:
(7*1)+(6*3)+(5*1)+(4*9)+(3*5)+(2*5)+(1*2)=93
93 % 10 = 3
So 13195-52-3 is a valid CAS Registry Number.

13195-52-3SDS

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 4-nitro-2-phenylsulfanylthiophene

1.2 Other means of identification

Product number -
Other names 4-nitro-2-phenylsulfanyl-thiophene

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:13195-52-3 SDS

13195-52-3Upstream product

13195-52-3Downstream Products

13195-52-3Relevant articles and documents

Kinetic Study of Substituent Effects on the Mechanism of β-Elimination of Arenethiol from trans-2,3-Bis-(arylthio)-4-nitro-2,3-dihydrothiophenes in Toluene

Petrillo, Giovanni,Novi, Marino,Garbarino, Giacomo,Dell'Erba, Carlo

, p. 1741 - 1746 (2007/10/02)

The 2,3-dihydrothiophene derivatives (1b-f) readily undergo, in toluene, regiospecific tributylamine-promoted syn-elimination of arenethiol to give the 2-(arylthio)-4-nitrothiophenes (2b-f).For the rather complex kinetic behaviour displayed by each member of the series, a rationalisation is proposed based on a stability of the substrate's conjugate base sufficient to allow formation of non-negligible concentrations of an intermediate ion pair along the reaction co-ordinate.The system allows direct conclusions to be drawn concerning the leaving-group expulsion step: an advanced extent of bond cleavage between carbon and the leaving group can be postulated in the transition state.

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