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Methyl Bicyclo<4.2.0>octa-1,3,5-triene-2-carboxylate is a chemical compound with the molecular formula C10H10O2. It is a derivative of bicycloocta-1,3,5-triene, a bicyclic aromatic hydrocarbon, with a carboxylate group attached to the 2-position and a methyl group at the carboxylate carbon. Methyl Bicyclo<4.2.0>octa-1,3,5-triene-2-carboxylate is known for its unique structure and potential applications in organic synthesis, particularly as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its chemical properties and reactivity make it a valuable compound for researchers and chemists in the field of organic chemistry.

1708-59-4

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1708-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1708-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1708-59:
(6*1)+(5*7)+(4*0)+(3*8)+(2*5)+(1*9)=84
84 % 10 = 4
So 1708-59-4 is a valid CAS Registry Number.

1708-59-4Downstream Products

1708-59-4Relevant academic research and scientific papers

Cyclization of benzyne-tethered alkyllithiums: Preparation of 3-substituted benzocyclobutenes and 5-substituted tetralins

Bailey, William F.,Longstaff, Sarah C.

, p. 6899 - 6901 (1999)

A five-step, one-pot preparation of isomerically pure 3-substituted benzocyclobutenes or 5-substituted tetralins in 20-40% yield from the appropriate α-(2-fluorophenyl)-ω-iodoalkane, involving generation and subsequent 4-or 6-exo cyclization of a benzyne-tethered alkyllithium, is described.

Bicycloocta-1,3,5-triene: 2-Mono- and 2,5-Disubstituted Derivatives via Highly Regioselective Lithiation of Its Cr(CO)3 Complex and via Reductive Silylation / Oxidation

Kuendig, E. Peter,Perret, Celia,Rudolph, Bruno

, p. 1970 - 1979 (1990)

Treatment of 6-(bicycloocta-1,3,5-triene)>tricarbonylchromium(0) (2) with BuLi or lithium 2,2,6,6-tetramethylpiperidinide (TMPLi) gives rise to a highly regioselective deprotonation at C(2).Subsequent reaction with electrophiles (6 exa

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