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91817-61-7

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91817-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91817-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,1 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91817-61:
(7*9)+(6*1)+(5*8)+(4*1)+(3*7)+(2*6)+(1*1)=147
147 % 10 = 7
So 91817-61-7 is a valid CAS Registry Number.

91817-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(8-methyl-8-azabicyclo[3.2.1]octan-3-ylidene)acetonitrile

1.2 Other means of identification

Product number -
Other names 3-cyanomethylene-8-methyl-8-azabicyclo[3.2.1]octane

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:91817-61-7 SDS

91817-61-7Downstream Products

91817-61-7Relevant articles and documents

Tryptophan-derived butyrylcholinesterase inhibitors as promising leads against Alzheimer's disease

Meden, An?e,Knez, Damijan,Juki?, Marko,Brazzolotto, Xavier,Gr?i?, Marija,Pi?lar, Anja,Zahirovi?, Abida,Kos, Janko,Nachon, Florian,Svete, Jurij,Gobec, Stanislav,Gro?elj, Uro?

supporting information, p. 3765 - 3768 (2019/04/01)

We have identified tryptophan-based selective nanomolar butyrylcholinesterase (BChE) inhibitors. They are defined according to their chemical modularity, novel binding mode revealed by five solved crystal structures with human BChE, low cytotoxicity, and predicted permeability of the blood-brain barrier. Altogether, these factors indicate their potential as unique lead compounds for symptomatic therapy against Alzheimer's disease.

Model Compounds for the Study of Spectroscopic Properties of Visual Pigments and Bacteriorhodopsin

Baasov, Timor,Sheves, Mordechai

, p. 7524 - 7533 (2007/10/02)

A series of modified retinals bearing nonconjugated positive charges along the polyene were synthesized.It was found that nonconjugated charges shifted the absorption maxima of retinal chromophore as well as protonated retinal Schiff bases.The magnitude of shift observed in bacteriorhodopsin (bR), 5170 cm-1, could be found in our models by the additivity of two factors: (1) interaction through space with a positive charge located in the vicinity of the ring operating in nonprotic solvents, provided that the interaction between the charge and its counteranion is weakened by a homoconjugation effect; (2) weakening the interaction of the Schiff base positively charged nitrogen with its counteranion.A shift of ca. 5000 cm-1 can also be achieved by interaction through space with two nonconjugated positive charges.The absorption maximum of protonated retinal Schiff base is influenced significantly by an interaction with a nonconjugated charge located in the vicinity of the ring moiety or carbon 9.The influence of a charge located in the vicinity of carbon 12 and carbon 14 is minor.Nonconjugated positive charges have a remarkable effect on C=C stretching frequencies as well.It is suggested that the different C=C stretching frequencies found in bR, visual pigments, as well as their photochemically induced intermediates, may originate from interaction with external charges, the C=N+ stretching frequency does no exhibit similar sensitivity to external nonconjugated charges, and it is practically unaffected by them.

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