Cas 340291-00-1,Isobutyric acid (1S,4R,5R)-4-(6-benzoylamino-purin-9-yl)-5-(2-isobutyryloxy-ethyl)-2-isobutyryloxymethyl-cyclopent-2-enylmethyl ester

340291-00-1

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Basic information

Product Name: Isobutyric acid (1S,4R,5R)-4-(6-benzoylamino-purin-9-yl)-5-(2-isobutyryloxy-ethyl)-2-isobutyryloxymethyl-cyclopent-2-enylmethyl ester
Synonyms:
CAS NO:340291-00-1
Molecular Formula:
Molecular Weight: 619.718
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Isobutyric acid (1S,4R,5R)-4-(6-benzoylamino-purin-9-yl)-5-(2-isobutyryloxy-ethyl)-2-isobutyryloxymethyl-cyclopent-2-enylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Isobutyric acid (1S,4R,5R)-4-(6-benzoylamino-purin-9-yl)-5-(2-isobutyryloxy-ethyl)-2-isobutyryloxymethyl-cyclopent-2-enylmethyl ester(340291-00-1)
EPA Substance Registry System: Isobutyric acid (1S,4R,5R)-4-(6-benzoylamino-purin-9-yl)-5-(2-isobutyryloxy-ethyl)-2-isobutyryloxymethyl-cyclopent-2-enylmethyl ester(340291-00-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 340291-00-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 340291-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,2,9 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 340291-00:
(8*3)+(7*4)+(6*0)+(5*2)+(4*9)+(3*1)+(2*0)+(1*0)=101
101 % 10 = 1
So 340291-00-1 is a valid CAS Registry Number.

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340291-00-1Relevant academic research and scientific papers

Synthesis of aucubovir II, a new carbocyclic nucleoside analog

Bianco, Armandodoriano,Celletti, Lucia,Mazzei, Raffaele Antonio,Umani, Floriana

, p. 1331 - 1334 (2001)

The synthesis of a new carbocyclic nucleoside starting from aucubin, a natural methylcyclopentanoid monoterpene, has been performed, allowing the preparation of aucubovir II, a carbocyclic nucleoside analog with a highly functionalized cyclopentane ring. The stereocontrol of the coupling reaction was complete, utilizing the procedure described by Vorbrueggen with a purinic base.

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