Cas 252863-65-3,1-Naphthalenol, 2-butyl-4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

252863-65-3

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Basic information

Product Name: 1-Naphthalenol, 2-butyl-4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
Synonyms:
CAS NO:252863-65-3
Molecular Formula: C21H29BO4
Molecular Weight:
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-Naphthalenol, 2-butyl-4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1-Naphthalenol, 2-butyl-4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(252863-65-3)
EPA Substance Registry System: 1-Naphthalenol, 2-butyl-4-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(252863-65-3)

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: 252863-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 252863-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,8,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 252863-65:
(8*2)+(7*5)+(6*2)+(5*8)+(4*6)+(3*3)+(2*6)+(1*5)=153
153 % 10 = 3
So 252863-65-3 is a valid CAS Registry Number.

252863-65-3Upstream product

159087-40-8 2-hex-1-ynyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

252863-65-3Downstream Products

29366-46-9 3-n-butyl-2-hydroxy-1,4-naphthoquinone

252863-65-3Relevant academic research and scientific papers

A novel and highly regioselective Cr-mediated route to functionalised quinone boronic ester derivatives

Davies, Mark W.,Johnson, Christopher N.,Harrity, Joseph P. A.

, p. 2107 - 2108 (1999)

A novel and highly regioselective route to quinone boronic ester derivatives has been developed using a Fischer carbene mediated benzannulation process.

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