Cas 155899-89-1,2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester

155899-89-1

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Basic information

Product Name: 2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester
Synonyms: 2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester
CAS NO:155899-89-1
Molecular Formula:
Molecular Weight: 394.532
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: 2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester(155899-89-1)
EPA Substance Registry System: 2-[(R)-5-[(S)-2-Hydroxy-3-((R)-toluene-4-sulfinyl)-propyl]-dihydro-furan-(2E)-ylidene]-propionic acid tert-butyl ester(155899-89-1)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 155899-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155899-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 155899-89:
(8*1)+(7*5)+(6*5)+(5*8)+(4*9)+(3*9)+(2*8)+(1*9)=201
201 % 10 = 1
So 155899-89-1 is a valid CAS Registry Number.

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155899-89-1Relevant academic research and scientific papers

A short asymmetric synthesis of (+)-nonactic acid and (-)-8-epi-nonactic acid induced by a chiral sulfoxide group

Solladie,Dominguez

, p. 3898 - 3901 (2007/10/02)

A short enantioselective synthesis of (+)-(2S,3S,6R,8R)-nonactic acid and (-)-(2R,3R,6S,8R)-epinonactic acid is described. The key step was the stepwise stereoselective reduction of the triketo sulfoxide B without any protective group on the different carbonyls.

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