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4-(3-hydroxypropyl)tetrahydro-1H,5H-pyrazolo[1,2-a]pyrazol-4-ium is a complex organic compound with the molecular formula C8H16N3O. It is a derivative of pyrazolo[1,2-a]pyrazol, a bicyclic heterocyclic compound consisting of a pyrazole ring fused to a pyrazoline ring. The compound is characterized by the presence of a 3-hydroxypropyl group attached to the 4-position of the pyrazolo[1,2-a]pyrazol core. This hydroxyalkyl chain contributes to the compound's polarity and solubility properties. The compound may have potential applications in medicinal chemistry or as a building block for more complex molecules, but its specific uses and properties would require further investigation and characterization.

66314-45-2

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66314-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66314-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,1 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66314-45:
(7*6)+(6*6)+(5*3)+(4*1)+(3*4)+(2*4)+(1*5)=122
122 % 10 = 2
So 66314-45-2 is a valid CAS Registry Number.

66314-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,2,3,5,6,7-hexahydropyrazolo[1,2-a]pyrazol-4-ium-4-yl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(3-hydroxypropyl)-1,5-diazabicyclo<3.3.0>octanium 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:66314-45-2 SDS

66314-45-2Downstream Products

66314-45-2Relevant academic research and scientific papers

Reductive cleavage of Propellane-type Hydrazinium Dications as a Route to Medium-sized Ring Bicyclic Diamines with Bridgehead Nitrogen Atoms

Alder, Roger W.,Sessions, Richard B.,Bennet, Andrew J.,Moss, Richard E.

, p. 603 - 610 (2007/10/02)

Procedures are described for the preparation of 1,5-diazoniatricyclodecane (9), 1,5-diazoniatricycloundecane (10), 1,6-diazoniatricyclododecane (11), 1,6-diazoniatricyclotridecane (12), and 1,6-diazoniatricyclotetradecane (13) salts by the alkylation of 1,5-diazabicyclooctane and 1,6-diazabicyclodecane with suitable difunctional molecules XmY.The central N-N bond of these propellane-type hydrazinium dications may be cleaved by a variety of reducing agents to yield the bicyclic diamines 1,5-diazabicyclodecane (21), 1,5-diazabicycloundecane (22), 1,6-diazabicyclo-dodecane (23), 1,6-diazabicyclotridecane (24), and 1,6-diazabicyclotetradecane (25).The scope and limitations of this synthetic route to medium-sized ring bicyclic diamines are discussed.

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