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848245-21-6

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848245-21-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848245-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,2,4 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 848245-21:
(8*8)+(7*4)+(6*8)+(5*2)+(4*4)+(3*5)+(2*2)+(1*1)=186
186 % 10 = 6
So 848245-21-6 is a valid CAS Registry Number.

848245-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [RuCl2(triphenylphosphine)2(perhydroazepine)]

1.2 Other means of identification

Product number -
Other names [RuCl2(PPh3)2(piperidine)]

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:848245-21-6 SDS

848245-21-6Downstream Products

848245-21-6Relevant articles and documents

Benefits of donor solvents as additive on ROMP of norbornene catalyzed by amine Ru complexes

Matos, José Milton E.,Lima-Neto, Benedito S.

, p. 233 - 238 (2005)

With the aim of understanding the influence of donor solvents on the reactivity of the amine complexes [RuCl2(PPh3) 2(piperidine)] (1) and [RuCl2(PPh3) 2(imidazole)2] (2) in the presence of ethyldiazoacetate, and on the properties of the resulting polymer, a ring opening metathesis polymerization of norbornene was carried out in the presence of small amounts of common solvents such as additives (isopropanol, THF, N,N-dimethylformamide, 2,6-lutidine, isopropanethiol, acetonitrile, dimethyl sulfoxide, NEt 3, NH2Me and pyridine). From observations, typical coordinating solvents like DMSO, NEt3, NH2Me and pyridine, hardly affected the yields when either complex was employed. With other additives, the major advantage was the decrease in the polydispersity indices. On using complex 1 with 2,6-lutidine, observed values of Mw/M n were as low as 1.3, while the yield decreased from 99% to about 20-30% at RT for ~1 min in pure solution. In the case of complex 2, which is almost inactive to ROMP (19% at 50 °C for 5 min with Mw/M n = 6.30), the yield was three-fold (60% at 50 °C for 5 min with Mw/Mn = 1.95) compared to that of without THF. Further, the Mw/Mn was observed to decrease to 1.34 with 200 eq. of THF.

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