Cas 141883-99-0,Hydroxy-(5-methyl-furan-2-yl)-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

141883-99-0

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Basic information

Product Name: Hydroxy-(5-methyl-furan-2-yl)-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms:
CAS NO:141883-99-0
Molecular Formula:
Molecular Weight: 294.391
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: Hydroxy-(5-methyl-furan-2-yl)-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Hydroxy-(5-methyl-furan-2-yl)-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(141883-99-0)
EPA Substance Registry System: Hydroxy-(5-methyl-furan-2-yl)-acetic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(141883-99-0)

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: 141883-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141883-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,8,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141883-99:
(8*1)+(7*4)+(6*1)+(5*8)+(4*8)+(3*3)+(2*9)+(1*9)=150
150 % 10 = 0
So 141883-99-0 is a valid CAS Registry Number.

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141883-99-0Relevant academic research and scientific papers

Unexpected Pathway of the High-Pressure Reaction Between 2-Methylfuran and Alkyl Glyoxylates

Jurczak, Janusz,Belniak, Stanislaw,Kozluk, Tomasz

, p. 271 - 274 (2007/10/02)

High-pressure reactions of 2-methylfuran with activated carbonyl compounds, n-butyl and (R)-menthyl glyoxylate are described.The reactions carried out in toluene under 11 kbar at 50 deg C afforded ca 1:1 mixtures of two regioisomeric products 4 and 5, which after benzylation were separated by column chromatography.

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