Cas 945496-08-2,2-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran

945496-08-2

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Basic information

Product Name: 2-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran
Synonyms: 2-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran
CAS NO:945496-08-2
Molecular Formula:
Molecular Weight: 534.659
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-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran(945496-08-2)
EPA Substance Registry System: 2-(4-tert-butyl-2-(diisopropylphosphino)-6-(diphenylphosphino)phenoxy)tetrahydro-2H-pyran(945496-08-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 945496-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945496-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,4,9 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 945496-08:
(8*9)+(7*4)+(6*5)+(5*4)+(4*9)+(3*6)+(2*0)+(1*8)=212
212 % 10 = 2
So 945496-08-2 is a valid CAS Registry Number.

945496-08-2Upstream product

945496-08-2Downstream Products

945496-08-2Relevant academic research and scientific papers

Syntheses of symmetric and unsymmetric 2,6-bis(phosphino)phenols

Beganskiene, Aldona,Nikishkin, Nicolai I.,Luck, Rudy L.,Urnezius, Eugenijus

, p. 656 - 663 (2007/10/03)

Compounds bearing the structural motif of 2,6-bis(phosphino)phenol have been synthesized via two general methods. Double lithium-halogen exchange occurred in low-temperature reactions of O-protected (by methyl- or tetrahydropyranyl groups) 2,6-dibromo-4-m

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