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745783-98-6

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745783-98-6 Usage

General Description

(1R,2R)-(-)-2-BENZYLOXYCYCLOHEXYL ISOTHIOCYANATE is a chemical compound with the molecular formula C15H19NOS. It is an isothiocyanate derivative, which is a functional group containing a sulfur atom bonded to an isocyanate group. (1R,2R)-(-)-2-BENZYLOXYCYCLOHEXYL ISOTHIOCYANATE is commonly used in organic synthesis as a reagent for the introduction of the isothiocyanate group into various organic molecules. It is often utilized in the preparation of pharmaceuticals, agrochemicals, and materials science. The (1R,2R)-(-) stereochemistry indicates that the compound has a specific spatial arrangement of its atoms, which can influence its reactivity and biological activity. (1R,2R)-(-)-2-BENZYLOXYCYCLOHEXYL ISOTHIOCYANATE is a valuable tool for synthetic chemists and researchers working in various scientific fields.

Check Digit Verification of cas no

The CAS Registry Mumber 745783-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,7,8 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 745783-98:
(8*7)+(7*4)+(6*5)+(5*7)+(4*8)+(3*3)+(2*9)+(1*8)=216
216 % 10 = 6
So 745783-98-6 is a valid CAS Registry Number.

745783-98-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L20316)  (1R,2R)-(-)-2-Benzyloxycyclohexyl isothiocyanate, 97%   

  • 745783-98-6

  • 1g

  • 746.0CNY

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745783-98-6Downstream Products

745783-98-6Relevant articles and documents

Synthesis and antitumor activity of optically active thiourea and their 2-aminobenzothiazole derivatives: A novel class of anticancer agents

Manjula,Malleshappa Noolvi,Vipan Parihar,Manohara Reddy,Ramani, Vijay,Gadad, Andanappa K.,Singh, Gurdial,Gopalan Kutty,Mallikarjuna Rao

experimental part, p. 2923 - 2929 (2009/09/30)

A novel series of optically active 2-aminobenzothiazole derivatives were synthesized by reaction of optically active amine (I) with thiophosgene to obtain optically active isothiocyanates (IIa-h) which on condensation with 4-fluoro-3-chloro aniline (III)

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