Cas 1437786-66-7,2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine

1437786-66-7

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Basic information

Product Name: 2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
Synonyms: 2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine
CAS NO:1437786-66-7
Molecular Formula:
Molecular Weight: 398.121
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: 2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(1437786-66-7)
EPA Substance Registry System: 2-(2-phenyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)ethyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine(1437786-66-7)

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: 1437786-66-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1437786-66-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,7,7,8 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1437786-66:
(9*1)+(8*4)+(7*3)+(6*7)+(5*7)+(4*8)+(3*6)+(2*6)+(1*6)=207
207 % 10 = 7
So 1437786-66-7 is a valid CAS Registry Number.

1437786-66-7Upstream product

479-27-6 naphthalene-1,8-diamine

1437786-66-7Downstream Products

1245706-89-1 2,3-dihydro-2-(2-phenylethyl)-1H-naphtho[1,8-de]-1,3,2-diazaborine

1437786-66-7Relevant academic research and scientific papers

A Boron Activating Effect Enables Cobalt-Catalyzed Asymmetric Hydrogenation of Sterically Hindered Alkenes

Chirik, Paul J.,Krautwald, Simon,Pabst, Tyler P.,Viereck, Peter

, p. 3923 - 3930 (2020)

Unsymmetric 1,1-diboryl alkenes bearing one -[BPin] (BPin = pinacolatoboryl) and one -[BDan] (BDan = 1,8-diaminonaphthalatoboryl) substituent each were hydrogenated in high yield and enantioselectivity using C1-symmetric pyridine(diimine) (PDI)

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