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62898-68-4

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62898-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62898-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62898-68:
(7*6)+(6*2)+(5*8)+(4*9)+(3*8)+(2*6)+(1*8)=174
174 % 10 = 4
So 62898-68-4 is a valid CAS Registry Number.

62898-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name α-phthalimido-m-tolunitrile

1.2 Other means of identification

Product number -
Other names N-(3-cyanobenzyl)phthalimide

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:62898-68-4 SDS

62898-68-4Relevant articles and documents

Designed double-strand DNA cleavage with chelate-appended porphyrins

Groves, John T.,Matsunaga, Akio

, p. 1595 - 1600 (1996)

The first example of DNA double-strand cleavage mediated by a synthetic porphyrin is described. Two new porphyrins, each with two metal complexing appendages, were shown to mediate the oxidative double-strand cleavage of pBR322 plasmid DNA. By contrast, a porphyrin with one appendage was found to mediate only single-strand breaks.

Syntheses of Quadruply Two- And Three-Atom, Aza-Bridged, Cofacial Bis(5,10,15,20-tetraphenylporphyrins)

Bookser, Brett C.,Bruice, Thomas C.

, p. 4208 - 4218 (2007/10/02)

Several syntheses for quadruply aza-bridged, cofacial bis(5,10,15,20-tetraphenylporphyrins) were investigated. Reaction of 5,10,15,20-tetrakis(α-bromo-m-tolyl)porphyrin (2) with p-toluenesulfonamide or cyanamide and Cs2CO3 at high dilution in dimethylformamide produced the tosyl and cyano dimers 3a and 3b in 8% yield each. The method of choice was the reaction of porphyrin 2 with tosylamido porphyrin 5a under the same conditions to give dimer 3a in 38% yield. Biphenyl radical anion induced desulfonylation of 3a provided the amino dimer 3c (41%). Reaction of porphyrin 2 with tosylamido porphyrin 13 provided the dimer 14 (of reduced bridge length) in 1% yield. Other methods for the synthesis of 3a and 3c are also discussed. UV/vis and 1H NMR spectroscopic results suggest an eclipsed "screwed-down" preferred conformation for these dimers, and molecular models are used to illustrate this conformational possibility. (1) Several terms have been used to describe the orientation of one porphyrin ring parallel and coplanar on top of another (i.e., strati by Kagen,5b face to face by Collman,5a and cofacial by Chang3b). Whereas the term cofacial is now generally the most commonly used descriptor, we prefer the usage of strati (from stratum, Latin for covering) for the specific naming of compounds, since it allows for more detailed structural information than simple letter-number shorthand abreviations. Moreover, a new shorthand naming system will be presented in the body of this account,17 which derives naturally from the strati terminology used in the Experimental Section.

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