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The chemical compound "(1R,2R,6S,7S,10S)-10-(6-Bromo-hexyl)-8,9-dimethyl-4-phenyl-10-thioxo-4-aza-10λ5-phospha-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione" is a complex, chiral molecule with a unique structure. It features a phosphorus atom at its core, which is part of a four-membered azaphospholidine ring. The molecule has a tricyclic decane framework with a thioketal group at position 10, and it is further characterized by the presence of a 6-bromohexyl chain attached to the phosphorus. The compound also includes two methyl groups at positions 8 and 9, and a phenyl group at position 4. The stereochemistry is specified by the R,S notation, indicating the specific three-dimensional arrangement of the atoms around the chiral centers. (1R,2R,6S,7S,10S)-10-(6-Bromo-hexyl)-8,9-dimethyl-4-phenyl-10-thioxo-4-aza-10λ5-phospha-tricyclo[5.2.1.02,6]dec-8-ene-3,5-dione is likely to have specific applications in fields such as pharmaceuticals or materials science, where its unique structure could confer particular properties.

78870-66-3

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78870-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78870-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,7 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78870-66:
(7*7)+(6*8)+(5*8)+(4*7)+(3*0)+(2*6)+(1*6)=183
183 % 10 = 3
So 78870-66-3 is a valid CAS Registry Number.

78870-66-3Downstream Products

78870-66-3Relevant academic research and scientific papers

SOME USES OF PHOSPHOLES IN GENERAL SYNTHETIC ORGANOPHOSPHORUS CHEMISTRY

Mathey, F.

, p. 101 - 104 (2007/10/02)

The uses of phospholes for building phosphorins, carbon-phosphorus saturated heterocycles and phosphinidene generators are described.

New Method for Building Carbon-Phosphorus Heterocycles

Holand, Serge,Mathey, Francois

, p. 4386 - 4389 (2007/10/02)

The photolysis of 1-substituted 3,4-dimethylphosphole sulfides-N-phenylmaleimide cycloadducts in alcohols (R'OH) has been found to proceed with high yields whatever the nature of the R substituent.It provides a ready access to the almost unknown phosphinothioates RP(S)(H)OR'.When R = (CH2)nBr the phosphinothioates thus obtained are readily cyclized by NaH in THF.Five-, six-, and seven-membered rings have been obtained in this way.

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