Cas 145103-85-1,((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester

145103-85-1

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Basic information

Product Name: ((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester
Synonyms: ((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester
CAS NO:145103-85-1
Molecular Formula:
Molecular Weight: 264.321
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: ((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(145103-85-1)
EPA Substance Registry System: ((2S,4R,5S)-4-Hydroxy-5-phenethyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(145103-85-1)

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: 145103-85-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145103-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,0 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145103-85:
(8*1)+(7*4)+(6*5)+(5*1)+(4*0)+(3*3)+(2*8)+(1*5)=101
101 % 10 = 1
So 145103-85-1 is a valid CAS Registry Number.

145103-85-1Upstream product

145103-82-8 (Z)-3-Hydroxy-8-phenyl-oct-5-enoic acid methyl ester

145103-85-1Downstream Products

145103-85-1Relevant academic research and scientific papers

IODINE-INDUCED CYCLISATIONS OF (E)- AND (Z)-3-HYDROXY-5-ALKENOATES: STEREOSELECTIVE APPROACHES TO TRISUBSTITUTED TETRAHYDROFURANS

Bennett, Frank,Bedford, Simon B.,Bell, Kathryn E.,Fenton, Garry,Knight, David W.,Shaw, Duncan

, p. 6507 - 6510 (1992)

Iodoetherification of the (Z)-3-hydroxy-5-alkenoates 4 leads exclusively to the hydroxy-tetrahydrofurans 5 whereas similar cyclisations of the corresponding (E)-isomers give largely the iodo-tetrahydrofurans .

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