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2,5-diazabicyclo[2.2.2]octane-2,5-diylbis(phenylmethanone) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1098-69-7

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1098-69-7 Usage

Properties

Heterocyclic compound
White crystalline solid
Characteristic amine-like odor
Highly soluble in organic solvents

Uses

Catalyst in chemical reactions
Stabilizer in processes
Production of polyurethanes
Pharmaceuticals
Curing agent for epoxy resins

Role in organic chemistry

Strong base
Nucleophilic catalyst

Check Digit Verification of cas no

The CAS Registry Mumber 1098-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1098-69:
(6*1)+(5*0)+(4*9)+(3*8)+(2*6)+(1*9)=87
87 % 10 = 7
So 1098-69-7 is a valid CAS Registry Number.

1098-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-benzoyl-2,5-diazabicyclo[2.2.2]octan-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2,5-Diazabicyclo<2.2.2>octan-dibenzoat

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:1098-69-7 SDS

1098-69-7Upstream product

1098-69-7Downstream Products

1098-69-7Relevant academic research and scientific papers

Antifilarial agents. Diazabicyclooctanes and diazabicycloheptanes as bridged analogs of diethylcarbamazine

Sturm,Henry,Thompson,et al.

, p. 481 - 487 (2007/10/04)

Twelve analogs of diethylcarbamazine (DEC) were prepared by acylation of 3 and 8 methyl 3,8 diazabicyclo[3.2.1]octane, 2 methyl 2,5 diazabicyclo[2.2.2]octane, and 2 methyl 2,5 diazabicyclo[2.2.1]heptane with diethylcarbamyl chloride, ethyl chloroformate, ethyl isocyanate, and cyclohexanecarbonyl chloride. These compounds are formally derived from DEC in possessing two or one carbon bridges over the piperazine ring. When evaluated against Litomosoides carinii in the gerbil, all compounds strongly suppressed blood microfilaremia levels but did not affect the adult worms. Several compounds were nearly equivalent to DEC in activity. The results are discussed in terms of molecular model studies and receptor site theory.

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