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23418-91-9

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23418-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23418-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,4,1 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23418-91:
(7*2)+(6*3)+(5*4)+(4*1)+(3*8)+(2*9)+(1*1)=99
99 % 10 = 9
So 23418-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H19B/c1-2-6-12(7-3-1)15-13-8-4-9-14(15)11-5-10-13/h1-3,6-7,13-14H,4-5,8-11H2

23418-91-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-phenyl-9-borabicyclo[3.3.1]nonane

1.2 Other means of identification

Product number -
Other names phenyl-9-BBN

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23418-91-9 SDS

23418-91-9Relevant articles and documents

DYNAMIC NMR SPECTROSCOPY OF THE TETRAVALENT ORGANOBORATE COMPOUNDS. SYNTHESIS AND SOME UNIQUE FEATURES OF ORGANOBORATES CONTAINING THE C6H4CH2NMe2-2 LIGAND

Kalbarczyk, E.,Pasynkiewicz, S.

, p. 119 - 132 (1985)

Novel borates (ArBMe3)Li*OEt2 (I), (ArBEt)Li*OEt2 (II) and (BArPh-9-BBn)Li*OEt2 (III) (Ar=C6H4NMe2-2, 9-BBN=9-borabicyclononyl) were synthesized in the reactions of ArLi with BMe3, BEt3 and BPh-9-BBN, respectively.Detailed studies were made of 1H,

Palladium-catalyzed 1,3-diol fragmentation: Synthesis of ω-dienyl aldehydes

Kimura, Masanari,Mori, Masahiko,Tamaru, Yoshinao

, p. 4504 - 4506 (2007)

2-(1′-Hydroxy-2′-propenyl)cycloalkan-1-ols 1 undergo dehydrative C1-C2 bond cleavage and provide ω-dienyl aldehydes 2 under the catalysis of Pd(0) and 9-phenyl-9-BBN. The Royal Society of Chemistry.

New Method for the Synthesis of Organoboranes

Whiteley, Chris G.

, p. 5 - 6 (1981)

Mixed organoboranes can be conveniently prepared in a single stage by treatment of a dialkylborane with various lithium dialkyl- or diaryl-cuprates.

Suzuki-miyaura cross-coupling reactions of unactivated alkyl halides catalyzed by a nickel pincer complex

Di Franco, Thomas,Boutin, Nicolas,Hu, Xile

, p. 2949 - 2958 (2013/11/06)

A nickel(II) pincer complex, [(MeN2N)Ni-Cl], was used to catalyze alkyl-alkyl and alkyl-aryl Suzuki-Miyaura coupling reactions of unactivated alkyl halides. The coupling of 9-alkyl-9-borabicyclo[3.3.1]nonane and 9-phenyl-9-borabicyclo[3.3.1]nonane reagents with alkyl halides was achieved in modest to good yields. The reactions tolerated a variety of useful functional groups including ester, ether, furan, thioether, acetal, and Boc groups. Georg Thieme Verlag Stuttgart, New York.

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