Cas 1171867-50-7,1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one

1171867-50-7

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Basic information

Product Name: 1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one
Synonyms: 1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one
CAS NO:1171867-50-7
Molecular Formula:
Molecular Weight: 306.402
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: 1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one(1171867-50-7)
EPA Substance Registry System: 1-((4R,6S)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)propan-2-one(1171867-50-7)

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: 1171867-50-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1171867-50-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,1,8,6 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1171867-50:
(9*1)+(8*1)+(7*7)+(6*1)+(5*8)+(4*6)+(3*7)+(2*5)+(1*0)=167
167 % 10 = 7
So 1171867-50-7 is a valid CAS Registry Number.

1171867-50-7Upstream product

171524-04-2 (4R,6S)-4-allyl-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxane

1171867-50-7Downstream Products

1171867-50-7Relevant academic research and scientific papers

An asymmetric synthesis of the polyol fragment of the polyene macrolide antibiotic RK-397

Fu, Fan,Loh, Teck-Peng

, p. 3530 - 3533 (2009)

A highly convergent and asymmetric synthesis of the C11-C31 polyol fragment of RK-397 as a single isomer is accomplished via a catalytic enantioselective hetero-Diels-Alder reaction and an intermolecular olefin cross-metathesis as key steps.

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