Cas 126862-03-1,(2S,3R,5S)-5-Hexyl-2-hydroxy-2-methyl-tetrahydro-furan-3-carboxylic acid methyl ester

126862-03-1

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Basic information

Product Name: (2S,3R,5S)-5-Hexyl-2-hydroxy-2-methyl-tetrahydro-furan-3-carboxylic acid methyl ester
Synonyms:
CAS NO:126862-03-1
Molecular Formula:
Molecular Weight: 244.331
EINECS: N/A
Product Categories: N/A
Mol File: 126862-03-1.mol
Article Data: 1

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,3R,5S)-5-Hexyl-2-hydroxy-2-methyl-tetrahydro-furan-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,5S)-5-Hexyl-2-hydroxy-2-methyl-tetrahydro-furan-3-carboxylic acid methyl ester(126862-03-1)
EPA Substance Registry System: (2S,3R,5S)-5-Hexyl-2-hydroxy-2-methyl-tetrahydro-furan-3-carboxylic acid methyl ester(126862-03-1)

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: 126862-03-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126862-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126862-03:
(8*1)+(7*2)+(6*6)+(5*8)+(4*6)+(3*2)+(2*0)+(1*3)=131
131 % 10 = 1
So 126862-03-1 is a valid CAS Registry Number.

126862-03-1Upstream product

126862-03-1Downstream Products

126862-03-1Relevant articles and documents

COBALT(II) ACETATE PROMOTED ADDITION OF ACETOACETATE TO TERMINAL OLEFINS: A HIGHLY STEREOSELECTIVE SYNTHESIS OF 5-ALKYL-2-HYDROXY-2-METHYL-3-METHOXYCARBONYL TETRAHYDROFURANS

Iqbal, Javed,Kumar, T. K. Praveen,Manogaran, S.

, p. 4701 - 4702 (2007/10/02)

Methylacetoacetate and terminal olefins react in presence of Cobalt(II) acetate and Oxygen to give the title compound(2) in a highly stereoselective manner and the structure of this compound is elucidated by 1H NMR simulation studies.

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