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3,4-Pyrrolidinediol,1-ethyl-,(3S,4S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

298688-65-0

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298688-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 298688-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,6,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 298688-65:
(8*2)+(7*9)+(6*8)+(5*6)+(4*8)+(3*8)+(2*6)+(1*5)=230
230 % 10 = 0
So 298688-65-0 is a valid CAS Registry Number.

298688-65-0Upstream product

298688-65-0Downstream Products

298688-65-0Relevant articles and documents

Synthesis of N-substituted (3S,4S)- and (3R,4R)-pyrrolidine-3,4-diols: Search for new glycosidase inhibitors

Lysek, Robert,Vogel, Pierre

, p. 3167 - 3181 (2007/10/03)

N-Substituted (3S,4S)- and (3R,4R)-pyrrolidine-3,4-diols 9 and 10, respectively, were derived from (+)-L-and (-)-D-tartaric acid, respectively. Compounds 9k, 91, and 9m with the N-substituents, BnNH(CH2) 2, 4-PhC6H4/

Polyhydroxypyrrolidine glycosidase inhibitors related to (+)-lentiginosine1

Cardona, Francesca,Goti, Andrea,Picasso, Sylviane,Vogel, Pierre,Brandi, Alberto

, p. 585 - 601 (2007/10/03)

(+)-Lentiginosine (14) and (7R)-7-hydroxylentiginosine (26), powerful inhibitors of amyloglucosidases, and their enantiomers were obtained in high overall yields by a multistep synthesis involving 1,3-dipolar cycloaddition of enantiopure tartaric acid derived pyrroline N-oxides. Structurally related (S,S)-3,4-dihydroxypyrrolidines 29-33 were synthesized as simpler models and tested towards 24 glycosidases.

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