Cas 186750-57-2,6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester

186750-57-2

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Basic information

Product Name: 6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester
Synonyms: 6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester
CAS NO:186750-57-2
Molecular Formula:
Molecular Weight: 454.561
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: 6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester(186750-57-2)
EPA Substance Registry System: 6-Hydroxy-4-(2-hydroxy-ethyl)-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-hexanoic acid ethyl ester(186750-57-2)

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: 186750-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 186750-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,7,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 186750-57:
(8*1)+(7*8)+(6*6)+(5*7)+(4*5)+(3*0)+(2*5)+(1*7)=172
172 % 10 = 2
So 186750-57-2 is a valid CAS Registry Number.

186750-57-2Upstream product

186750-56-1 3-Cyclopent-3-enyl-3-{2-[2-(4-methoxy-benzyloxy)-ethyl]-[1,3]dioxolan-2-yl}-2-methyl-propionic acid ethyl ester

186750-57-2Downstream Products

186750-57-2Relevant academic research and scientific papers

A stereoselective total synthesis of (±)-oppositol by a doubly diastereoselective intramolecular ester enolate alkylation

Kim, Deukjoon,Kim, In Ho

, p. 415 - 416 (1997)

The brominated terpene (±)-oppositol (1) has been synthesized utilizing a novel doubly diastereodifferentialing 'folding and allylic strain-controlled' intramolecular ester enolate alkylation.

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