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methyl (E)-6-<4-<oxy>-2H-thiopyran-2-yl>-2-hexenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148005-55-4

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148005-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148005-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,0,0 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 148005-55:
(8*1)+(7*4)+(6*8)+(5*0)+(4*0)+(3*5)+(2*5)+(1*5)=114
114 % 10 = 4
So 148005-55-4 is a valid CAS Registry Number.

148005-55-4Downstream Products

148005-55-4Relevant academic research and scientific papers

INTRAMOLECULAR DIELS-ALDER REACTIONS OF 2H-THIOPYRANS

Ward, Dale E.,Nixey, Thomas E.

, p. 947 - 950 (1993)

Intramolecular Diels-Alder reactions of a series of substrates with 4-triisopropylsilyloxy-2H-thiopyran as the diene and a dienophile attached to each of the four possible positions by a three carbon tether were examined.Key Words: intramolecular Diels-Alder, 2H-thiopyran diene, cis-diene

Intramolecular Diels-Alder reactions of 2H-thiopyran dienes

Ward, Dale E.,Nixey, Thomas E.,Gai, Yuanzhu,Hrapchak, Matthew J.,Abaee, M. Saeed

, p. 1418 - 1436 (2007/10/03)

A systematic survey of IMDA reactions of 4-[tris(2-methylethyl)silyl]oxy-2H-thiopyran derivatives with potential dienophiles tethered at the C-2, C-3, C-5, and C-6 positions is presented. Cycloaddition was not observed with a C3 or C4 tether and an unactivated terminal olefin as dienophile. IMDA adducts could be obtained when dienophiles activated by a carbomethoxy group were employed. Compounds having the activated dienophile attached via a C3 tether to C-2 of the 2H-thiopyran gave adducts with high stereoselectivity. Substrates having the dienophile attached to C-3 with a C3 or C4 tether cyclized readily. With an (E)-enoate as the dienophile, the stereoselectivity was poor (endo:exo = 1.1-2.5:1) and essentially independent of reaction conditions (i.e., thermal vs. Lewis acid mediated). With the (Z)-enoate, a 7:1 mixture of endo:exo IMDA adducts was obtained under thermal conditions; with Lewis acid catalysis, isomerization of the dienophile was competitive with cycloaddition. Type II IMDA adducts were not observed with C-5 tethered substrates. Compounds having the dienophile attached to C-A via a C3 or a five-atom tether also failed to give IMDA adducts. No evidence for isomerization of the 2H-thiopyran dicnes by [1,5] sigmatropic rearrangement was observed. The endo adducts from IMDA reactions of the C-3 tethered substrates can be desulfurized to obtain synthetically useful trans-fused hydrindans and decalins with angular methyl groups.

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