Cas 1453285-82-9,(2S,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol

1453285-82-9

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Basic information

Product Name: (2S,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol
Synonyms: (2S,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol
CAS NO:1453285-82-9
Molecular Formula:
Molecular Weight: 414.542
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,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol(1453285-82-9)
EPA Substance Registry System: (2S,3S,5S)-1,5-bis(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-methylpentan-2-ol(1453285-82-9)

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: 1453285-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1453285-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,2,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1453285-82:
(9*1)+(8*4)+(7*5)+(6*3)+(5*2)+(4*8)+(3*5)+(2*8)+(1*2)=169
169 % 10 = 9
So 1453285-82-9 is a valid CAS Registry Number.

1453285-82-9Upstream product

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1453285-82-9Relevant academic research and scientific papers

Stereoselective total synthesis of (-)-brevisamide

Yadav,Reddy, N. Mallikarjuna,Rahman, Md. Ataur,Prasad,Reddy, B.V. Subba

, p. 8618 - 8625 (2013)

The stereoselective total synthesis of (-)-brevisamide, a novel marine cyclic ether alkaloid isolated from dinoflagellate karenia brevis is described. The key steps involved in this synthesis are the Sharpless asymmetric epoxidation and regioselective rin

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