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10002-30-9

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10002-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10002-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10002-30:
(7*1)+(6*0)+(5*0)+(4*0)+(3*2)+(2*3)+(1*0)=19
19 % 10 = 9
So 10002-30-9 is a valid CAS Registry Number.

10002-30-9SDS

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 S-pyridin-2-yl benzenecarbothioate

1.2 Other means of identification

Product number -
Other names thiobenzoic acid S-pyridin-2-yl 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:10002-30-9 SDS

10002-30-9Relevant articles and documents

Reductive Cleavage of Aromatic Disulfides Using a Polymer-Supported Phosphine Reagent

Amos, Richard A.,Fawcett, Shayne M.

, p. 2637 - 2639 (1984)

-

Corey,Clark

, p. 2875,2876 (1979)

S-(2-pyridinyl)-1,1,3,3-tetramethylthiouronium hexafluorophosphate. A new reagent for the synthesis of 2-pyridinethiol esters

Scardovi, Noemi,Garner, Philip P.,Protasiewicz, John D.

, p. 1633 - 1635 (2003)

(Matrix presented) A new thiouronium-based reagent for the synthesis of 2-pyridinethiol esters under non-nucleophilic conditions from the corresponding carboxylic acids was developed. The resulting procedure enables the preparation of previously unavailable α,β-unsaturated 2-pyridinethiol esters as well as their aliphatic and aromatic counterparts.

Cobalt-catalyzed acylation-reactions of (hetero)arylzinc pivalates with thiopyridyl ester derivatives

Lutter, Ferdinand H.,Grokenberger, Lucie,Hofmayer, Maximilian S.,Knochel, Paul

, p. 8241 - 8245 (2019/09/19)

A cobalt-catalyzed acylation reaction of various primary, secondary and tertiary alkyl, benzyl and (hetero)aryl S-pyridyl thioesters with (hetero)arylzinc pivalates is reported. The thioesters were prepared directly from the corresponding carboxylic acids under mild conditions, thus tolerating sensitive functional groups. Acylations of α-chiral S-pyridyl esters proceeded with very high stereoretention leading to optically enriched α-chiral ketones.

Photoinduced Dynamics of Bis-dipyrrinato-palladium(II) and Porphodimethenato-palladium(II) Complexes: Governing Near Infrared Phosphorescence by Structural Restriction

Riese, Stefan,Holzapfel, Marco,Schmiedel, Alexander,Gert, Ingo,Schmidt, David,Würthner, Frank,Lambert, Christoph

supporting information, p. 12480 - 12488 (2018/10/25)

Although superficially similar, the bis-dipyrrinato-palladium(II) complex 1 and the bridged porphodimethenato-palladium(II) complex 2 possess dramatically different structures in the ground state (proved by X-ray structure analysis) and in the singlet and

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