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(3aR,5S,6S,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxole-5-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82529-87-1

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82529-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82529-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,2 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82529-87:
(7*8)+(6*2)+(5*5)+(4*2)+(3*9)+(2*8)+(1*7)=151
151 % 10 = 1
So 82529-87-1 is a valid CAS Registry Number.

82529-87-1Downstream Products

82529-87-1Relevant articles and documents

Synthesis of (+)-altholactone, (+)-7-epi-altholactone, (?)-etharvensin, and (+)-alumheptolide-A using Pd-catalyzed carbonylation

Miyazawa, Yuki,Hattori, Yasunao,Makabe, Hidefumi

, p. 4024 - 4027 (2018/10/05)

Syntheses of (+)-altholactone isolated from Goniothalamus giganteus and its C-7 epimer (+)-7-epi-altholactone, (?)-etharvensin and (+)-alumheptolide-A were achieved. The lactone ring of these compounds was constructed using Pd-catalyzed carbonylation.

Effect of ring fusion stereochemistry on double bond geometry. Unexpected formation of nine-membered cyclic ether with E-configurated double bond through RCM

Ghosh, Subrata,Hossain, Md. Firoj,Malik, Chanchal K.,Maity, Soumitra

experimental part, p. 9159 - 9164 (2011/01/12)

Formation of a nine-membered cyclic ether with E-configurated double bond was observed during construction of 5-9-5 tricycles through RCM of dienes. Ring fusion stereochemistry in the products oxonenes was found to have profound influence on the olefin geometry. cis-anti-cis 5-9-5 tricycle was obtained with Z-configurated olefin while cis-syn-cis 5-9-5 system was obtained with E- as well as Z-configurated double bond with the former predominating.

Synthesis of pyrenolide D analogues

Robertson, Jeremy,Stevens, Kiri,Naud, Sébastien

scheme or table, p. 2083 - 2086 (2009/04/17)

We present a short, enantiospecific synthesis of four hydroxylated analogues of pyrenolide D from D-glucose based on furan oxidative spirocyclisation. Georg Thieme Verlag Stuttgart.

Regioselective deprotection of p-methoxybenzyl ethers of furanose derivatives

Bouzide, Abderrahim,Sauve, Gilles

, p. 2883 - 2886 (2007/10/03)

Reaction of per-p-methoxybenzylated hexofuranoses and pentofuranoses with either a catalytic amount of tin chloride dihydrate (SnCl2·2H2O) or 0.5-10% solution of trifluoroaoetic acid in dichloromethane afforded regioselectively the corresponding monosaccharide derivatives having a single free hydroxyl group at C(5) in good yields.

STEREOSELECTIVE SYNTHESIS OF THE MIDDLE (C10-C17) AND RIGHT (C18-C30) SEGMENTS, AND THEIR COUPLING TO COMPLETE A FORMAL SYNTHESIS OF THE POLYETHER ANTIBIOTIC SALINOMYCIN

Horita, Kiyoshi,Nagato, Satoshi,Oikawa, Yuji,Yonemitsu, Osamu

, p. 3253 - 3256 (2007/10/02)

The middle (C10-C17) and right (C18-C30) segments of the polyether antibiotic salinomycin were stereoselectively synthesized from D-glucose, D-mannitol, and ethyl L-lactate.Coupling of the two segments followed by construction of the bisketal ring system gave the C10-C30 segment, which was already converted to salinomycin by Kishy.

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