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80319-87-5

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80319-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80319-87-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,1 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80319-87:
(7*8)+(6*0)+(5*3)+(4*1)+(3*9)+(2*8)+(1*7)=125
125 % 10 = 5
So 80319-87-5 is a valid CAS Registry Number.

80319-87-5SDS

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 (2Z,6E,10E)-1-bromo-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraene

1.2 Other means of identification

Product number -
Other names 2Z,6E,10E-geranylgeranyl bromide

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:80319-87-5 SDS

80319-87-5Relevant articles and documents

THE PREPARATION AND REACTIONS OF BIS(PYRAZOLYL)PHENYLMETHANE COMPLEXES OF RHODIUM(I)

Leung, Ping Y.,Peterson, Louis K.

, p. 409 - 420 (2007/10/02)

The complexes x (I), (II), (III) and +Cl- (IV) have been prepared via the reactions of the bis-(pyrazolyl)phenylmethane ligands PhCH(H2pz)2 (LL; H2pz = pyrazolyl) and PhCH(Me2pz)2 (MeLL; Me2pz = 3,5-dimethylpyrazolyl) with 2 and 2 (cod = cyclooctadiene).Complex IV reacts with NaBPh4 to form +BPh4- (V).III and IV react with carbon monoxide to give +- (VI).Complexes I and III give neutral solutions in methanol, while II and IV behave as 1:2 and 1:1 electrolytes, respectively.The rhodium(I) centre is typically four-coordinate in I, II, IV-VI, and five-coordinate in III.The ligands LL and MeLL show bidentate chelating behaviour in all of the above complexes, with the exception of II, where LL bridges two different RhI moieties.Reactions with H2, HCl and Ph3P are described.Complex III functions as a homogeneous catalyst, in neutral methanolic solution, for the hydrogenation of olefins, but is ineffective for the hydrogenation of α,β-unsaturated aldehydes and ketones.

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