Cas 174589-67-4,Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester

174589-67-4

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Basic information

Product Name: Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester
Synonyms: Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester
CAS NO:174589-67-4
Molecular Formula:
Molecular Weight: 276.289
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: Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester(174589-67-4)
EPA Substance Registry System: Benzoic acid (3aR,4R,5R,6aS)-5-hydroxy-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester(174589-67-4)

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: 174589-67-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174589-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,8 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174589-67:
(8*1)+(7*7)+(6*4)+(5*5)+(4*8)+(3*9)+(2*6)+(1*7)=184
184 % 10 = 4
So 174589-67-4 is a valid CAS Registry Number.

174589-67-4Upstream product

174589-67-4Downstream Products

174474-86-3 Benzoic acid (3aR,4R,5R,6aS)-5-(tert-butyl-dimethyl-silanyloxy)-2-oxo-hexahydro-cyclopenta[b]furan-4-ylmethyl ester

174589-67-4Relevant academic research and scientific papers

Total Synthesis of 12-epi-PGF2α

Hwang, Seong-Woo,Adiyaman, Mustafa,Khanapure, Subhash P.,Rokach, Joshua

, p. 779 - 782 (1996)

A novel synthesis of 12-epi-PGF2α 5 is described. The key synthon 11, which has been used as a starting point for the synthesis, is produced by a radical cyclization process using thionocarbonate 9a. The radical cyclization of 9a to 11 has been studied in some detail.

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