Welcome to LookChem.com Sign In|Join Free

CAS

  • or

63074-07-7

Post Buying Request

63074-07-7 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

63074-07-7 Usage

Chemical Properties

colorless to yellow viscous liquid

Uses

1-?(Tetrahydro-?2-?furoyl)?-?piperazine (Terazosin EP Impurity N) has been used as a reactant for the preparation of pyrazol-3-propanoic acid derivatives as inhibitors of leukotriene biosynthesis in human neutrophils.

Check Digit Verification of cas no

The CAS Registry Mumber 63074-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63074-07:
(7*6)+(6*3)+(5*0)+(4*7)+(3*4)+(2*0)+(1*7)=107
107 % 10 = 7
So 63074-07-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O2/c12-9(8-2-1-7-13-8)11-5-3-10-4-6-11/h8,10H,1-7H2/p+1/t8-/m1/s1

63074-07-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L18704)  1-(2-Tetrahydrofuroyl)piperazine, 97%   

  • 63074-07-7

  • 5g

  • 364.0CNY

  • Detail
  • Alfa Aesar

  • (L18704)  1-(2-Tetrahydrofuroyl)piperazine, 97%   

  • 63074-07-7

  • 25g

  • 1255.0CNY

  • Detail
  • Sigma-Aldrich

  • (Y0000624)  Terazosin impurity N  European Pharmacopoeia (EP) Reference Standard

  • 63074-07-7

  • Y0000624

  • 1,880.19CNY

  • Detail
  • Aldrich

  • (CDS007497)  1-(tetrahydro-2-furoyl)-piperazine  AldrichCPR

  • 63074-07-7

  • CDS007497-1G

  • 966.42CNY

  • Detail

63074-07-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Tetrahydro-2-furoyl)piperazine

1.2 Other means of identification

Product number -
Other names 1-((tetrahydrofuran-2-yl)carbonyl)piperazine

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:63074-07-7 SDS

63074-07-7Relevant articles and documents

Why we might be misusing process mass intensity (PMI) and a methodology to apply it effectively as a discovery level metric

Monteith, Edward R.,Mampuys, Pieter,Summerton, Louise,Clark, James H.,Maes, Bert U. W.,McElroy, C. Robert

, p. 123 - 135 (2020)

Process mass intensity (PMI) is a key mass-based metric to evaluate the green credentials of an individual or sequence of reactions during process and chemical development. The increasing awareness to consider greenness as early as the initial discovery level, requires a set of parameters suitable to assess it at this stage of development, and guidelines to apply them correctly. This paper evaluates when and how PMI can be used in a correct manner. Different simulations for key reactions in the organic synthesis toolbox-i.e. amide bond formation and Mitsunobu reactions-illustrate that PMI can easily be misleading without due consideration of yield, concentration and molecular weight of reactants and product. A fair appraisal of the green potential of different methodologies therefore requires careful analysis of the examples and metrics data generated.

Molecular features of the prazosin molecule required for activation of Transport-P

da Silva, Joaquim Fernando Mendes,Walters, Marcus,Al-Damluji, Saad,Ganellin, C. Robin

, p. 7254 - 7263 (2008/12/23)

Closely related structural analogues of prazosin have been synthesised and tested for inhibition and activation of Transport-P in order to identify the structural features of the prazosin molecule that appear to be necessary for activation of Transport-P. So far, all the compounds tested are less active than prazosin. It is shown that the structure of prazosin appears to be very specific for the activation. Only quinazolines have been found to activate, and the presence of the 6,7-dimethoxy and 4-amino groups appears to be critically important.

Preparation of amides and quinazoline derivatives

-

, (2008/06/13)

The present invention relates to a process for the preparation of amides, comprising reacting amines with carboxylic acids in the presence of silicon amines. The present invention further relates to a process for the preparation of quinazoline derivatives, comprising reacting amines with carboxylic acids in the presence of silicon amines to obtain amides and contacting the resultant amides with quinazoline.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 63074-07-7