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2-((E)-7,7-Dimethoxy-4-phenylsulfanyl-hept-3-enyl)-2-methyl-[1,3]dithiane is a organic complex compound characterized by a unique molecular structure. It features a 1,3-dithiane core, which is a sulfur-containing heterocyclic compound consisting of two methane groups bridged by sulfur atoms. The molecule is further distinguished by an (E)-7,7-dimethoxy-4-phenylsulfanyl-hept-3-enyl group attached to the 2-position of the dithiane ring. The "E" configuration indicates the geometric isomerism of the double bond, with the phenyl and sulfanyl groups on the same side of the double bond. The dimethoxy groups suggest the presence two of methoxy substituents, which are -OCH3 groups, attached to the heptene chain. 2-((E)-7,7-Dimethoxy-4-phenylsulfanyl-hept-3-enyl)-2-methyl-[1,3]dithiane is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential reactivity.

87171-00-4

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87171-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87171-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,7 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87171-00:
(7*8)+(6*7)+(5*1)+(4*7)+(3*1)+(2*0)+(1*0)=134
134 % 10 = 4
So 87171-00-4 is a valid CAS Registry Number.

87171-00-4Relevant academic research and scientific papers

STRAIN AND SELECTIVITY: PARTNERS FOR ORGANIC SYNTHESIS

Trost, Barry M.

, p. 139 - 150 (2007/10/02)

The development of two new small-ring conjunctive reagents, (E)-2-(hydrohymethyl)cyclopropyl phenyl sulphide and 1,1-bis(benzenesulphonyl)cyclopropane, are reported.The former permits a synthesis of 2,4-disubstituted cyclobutanones and (E)-4-phenylthio-4-

BIFUNCTIONAL CYCLOPROPYL REAGENTS: A TOTAL SYNTHESIS OF 7-E,9-Z METHYL TRISPORATE B

Trost, Barry M.,Ornstein, Paul L.

, p. 2833 - 2836 (2007/10/02)

2-Hydroxymethylcyclopropyl phenyl sulfide combined with sulfenylation-dehydrosulfenylation permits a stereo- and chemoselective approach to trisporic acids.

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