Cas 1086975-22-5,potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate

1086975-22-5

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Basic information

Product Name: potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate
Synonyms: potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate
CAS NO:1086975-22-5
Molecular Formula:
Molecular Weight: 425.343
EINECS: N/A
Product Categories: N/A
Mol File: 1086975-22-5.mol
Article Data: 1

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: potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate(CAS DataBase Reference)
NIST Chemistry Reference: potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate(1086975-22-5)
EPA Substance Registry System: potassium 4-((5-(4-(1H-pyrrol-1-yl)phenyl)pentyloxy)methyl)phenyltrifluoroborate(1086975-22-5)

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: 1086975-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1086975-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,9,7 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1086975-22:
(9*1)+(8*0)+(7*8)+(6*6)+(5*9)+(4*7)+(3*5)+(2*2)+(1*2)=195
195 % 10 = 5
So 1086975-22-5 is a valid CAS Registry Number.

1086975-22-5Upstream product

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1086975-22-5Relevant articles and documents

Orthogonal reactivity in boryl-substituted organotrifluoroborates

Molander, Gary A.,Sandrock, Deidre L.

supporting information; experimental part, p. 15792 - 15793 (2009/05/15)

A method was developed for the hydroboration of alkenyl-containing organotrifluoroborates to generate dibora intermediates. The reactivity differences between organotrifluoroborates and trialkylboranes facilitated the cross-coupling of the borane moiety o

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