Cas 5831-38-9,5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one

5831-38-9

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Basic information

Product Name: 5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one
Synonyms: 5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one;5-Hydroxy-3-(hydroxymethyl)-7-oxabicyclo[4.1.0]hept-3-en-2-one
CAS NO:5831-38-9
Molecular Formula: C₇H₈O₄
Molecular Weight: 156.14
EINECS: N/A
Product Categories: N/A
Mol File: 5831-38-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 445.2±45.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.567±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 12.66±0.40(Predicted)
CAS DataBase Reference: 5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one(5831-38-9)
EPA Substance Registry System: 5,6-Epoxy-4-hydroxy-2-hydroxymethyl-2-cyclohexen-1-one(5831-38-9)

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: 5831-38-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 5831-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5831-38:
(6*5)+(5*8)+(4*3)+(3*1)+(2*3)+(1*8)=99
99 % 10 = 9
So 5831-38-9 is a valid CAS Registry Number.

5831-38-9Upstream product

5831-38-9Downstream Products

76596-39-9 (4R,5S,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-propylsulfanyl-cyclohex-2-enone

5831-38-9Relevant academic research and scientific papers

The synthesis of epi-epoxydon utilising the Baylis-Hillman reaction

Genski, Thorsten,Taylor, Richard J.K.

, p. 3573 - 3576 (2007/10/03)

(±)-epi-Epoxydon was synthesised by means of a triethylaluminium/tri-n-butylphosphine-catalysed Baylis-Hillman reaction between an O-protected epoxidised hydroxyquinol core and paraformaldehyde, constituting the first application of the Baylis-Hillman reaction to a highly functionalised β-substituted enone.

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