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89377-15-1

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89377-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89377-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89377-15:
(7*8)+(6*9)+(5*3)+(4*7)+(3*7)+(2*1)+(1*5)=181
181 % 10 = 1
So 89377-15-1 is a valid CAS Registry Number.

89377-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2-borolene

1.2 Other means of identification

Product number -
Other names 1-Phenyl-2-borolen

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:89377-15-1 SDS

89377-15-1Relevant articles and documents

KATALYTISCHE OLEFINISOMERISIERUNG VON 3-BOROLENEN; DER ERSTE ZUGANG ZU 2-BOROLENEN

Herberich, G. E.,Hessner, B.,Soehnen, D.

, p. C23 - C26 (1983)

The first 2-borolenes (Ia: R=NPr2i, Ib: R=Ph) have been obtained by catalytic isomerization of the corresponding 3-borolenes (II). 2 is used as catalyst precursor and slowly forms inactive (borole)rhodium comp

Synthesis and Reativity of 2-Borolenes and of 3-Borolenes

Herberich, Gerhard E.,Boveleth, Wilfried,Hessner, Bernd,Hostalek, Martin,Koeffer, Dieter P. J.,et al.

, p. 420 - 433 (2007/10/02)

C-Unsubstituted 3-borolenes C4H6BR (1) with alkyl, aryl, or dialkylamino substituents at boron are obtained by treating RBX2 (MeBBr2, C6H11BCl2, PhBCl2, o-TolBCl2, MesBCl2, Me2NBCl2, Et2NBCl2, (iPr)2NBCl2 with Mg(C4H6)*2THF in ether.Catalytic isomerization reactions produce the corresponding 2-borolenes C4H6BR (2) (R = Ph, NMe2, NEt2, N(iPr)2).Additional 2-borolenes (R = Me, Ph, Cl, OMe) can be obtained efficiently via 1-(diisopropylamino)-2-borolene (2h).Addition of organolithium reagents (LiMe, LiPh) and subsequent treatment with HCl in Et2O affords 1-R-2-borolenes (R = Me, Ph).Addition of polar reagents HX (HCl, MeOH) and subsequently of HCl in Et2O produces 1-heterosubstituted 2-borolenes (R = Cl, OMe).All borolenes are highly air- and watersensitive liquids of high reactivity.In addition to the usual characterization a number of simple crystalline derivatives, including some boratacyclopentene salts, are also described.

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