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(1S,2R,3E,4R)-(-)-(l)-menthyl 7-tert-butoxycarbonyl-3-[2'-(l)-menthyloxy-2'-oxoethylidene]-7-azabicyclo[2.2.1]heptane-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

219700-35-3

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219700-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219700-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,7,0 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 219700-35:
(8*2)+(7*1)+(6*9)+(5*7)+(4*0)+(3*0)+(2*3)+(1*5)=123
123 % 10 = 3
So 219700-35-3 is a valid CAS Registry Number.

219700-35-3Relevant academic research and scientific papers

New asymmetric transformation of optically active allene-1,3-dicarboxylate and its application to the formal asymmetric synthesis of (-)-epibatidine

Node, Manabu,Nishide, Kiyoharu,Fujiwara, Toshio,Ichihashi, Shogo

, p. 2363 - 2364 (1998)

A new efficient synthesis of di-(-)-L-menthyl (R)-allene-1,3-dicarboxylate [(R)-1] involving asymmetric transformation through epimerization-crystallization with the assistance of a catalytic amount of Et3N was developed; the highly endo-select

Synthesis of (-)-epibatidine and its derivatives from chiral allene-1,3-dicarboxylate esters

Kimura, Hiroyuki,Fujiwara, Toshio,Katoh, Takahiro,Nishide, Kiyoharu,Kajimoto, Tetsuya,Node, Manabu

, p. 399 - 402 (2007/10/03)

(-)-Epibatidine, an excellent candidate of non-opioidal anesthesia, was formally synthesized in short steps from di-(l)-menthyl (R)-allene-1,3- dicarboxylate that was facilely prepared as a single isomer by means of crystallization-induced asymmetric tran

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