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67-52-7

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67-52-7 Usage

Chemical Description

Barbituric acid is another small organic molecule that is used as a starting material for the synthesis of various drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 67-52-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67-52:
(4*6)+(3*7)+(2*5)+(1*2)=57
57 % 10 = 7
So 67-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H,(H3,5,6,7,8,9)

67-52-7 Well-known Company Product Price

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

  • (A10934)  Barbituric acid, 99%   

  • 67-52-7

  • 25g

  • 268.0CNY

  • Detail
  • Alfa Aesar

  • (A10934)  Barbituric acid, 99%   

  • 67-52-7

  • 100g

  • 342.0CNY

  • Detail
  • Alfa Aesar

  • (A10934)  Barbituric acid, 99%   

  • 67-52-7

  • 500g

  • 1013.0CNY

  • Detail
  • Alfa Aesar

  • (30748)  Barbituric acid, 98+%   

  • 67-52-7

  • 100g

  • 323.0CNY

  • Detail
  • Alfa Aesar

  • (30748)  Barbituric acid, 98+%   

  • 67-52-7

  • 500g

  • 871.0CNY

  • Detail
  • Sigma-Aldrich

  • (Y0000762)  Fluorouracil impurity A  European Pharmacopoeia (EP) Reference Standard

  • 67-52-7

  • Y0000762

  • 1,880.19CNY

  • Detail
  • USP

  • (1279019)  Fluorouracil Related Compound A  United States Pharmacopeia (USP) Reference Standard

  • 67-52-7

  • 1279019-25MG

  • 14,500.98CNY

  • Detail
  • Sigma-Aldrich

  • (185698)  Barbituricacid  ReagentPlus®, 99%

  • 67-52-7

  • 185698-25G

  • 372.06CNY

  • Detail
  • Sigma-Aldrich

  • (185698)  Barbituricacid  ReagentPlus®, 99%

  • 67-52-7

  • 185698-100G

  • 618.93CNY

  • Detail
  • Sigma-Aldrich

  • (185698)  Barbituricacid  ReagentPlus®, 99%

  • 67-52-7

  • 185698-500G

  • 1,482.39CNY

  • Detail

67-52-7SDS

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 barbituric acid

1.2 Other means of identification

Product number -
Other names Barbitursure

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:67-52-7 SDS

67-52-7Relevant articles and documents

-

Bolton

, p. 166,170 (1963)

-

Ultrasound-assisted rapid synthesis of 2-aminopyrimidine and barbituric acid derivatives

Bayramo?lu, Duygu,Kurtay, Gülbin,Güllü, Mustafa

, p. 649 - 658 (2020/02/11)

Novel, inexpensive, and relatively expeditious procedure to achieve the synthesis of different 2-aminopyrimidine and barbituric acid derivatives is presented here, starting from readily available compounds such as guanidine hydrochloride, urea, 1,3-dialkylurea, or thiourea. Under ultrasonic irradiation, base-driven (Na2CO3, NaOH, or NaOC2H5) heterocyclization reactions of the aforementioned substrates with diethyl malonate, diethyl-2-alkyl malonate, pentane-2,4-dione, or ethyl-3-oxobutanoate yielded corresponding products. Significant advantages of this sonochemical synthetic protocol with regard to the conventional thermal methods include easy reaction setup and work-up steps, reasonably mild conditions, shorter reaction times (~30 min) and comparably high product yields. The characterization of the synthesized compounds was based on melting points, FT-IR, GC-MS, 1H-NMR techniques, and the obtained data were also checked from the previously published studies.

Prebiotic Origin of Pre-RNA Building Blocks in a Urea “Warm Little Pond” Scenario

Menor Salván,Bouza, Marcos,Fialho, David M.,Burcar, Bradley T.,Fernández, Facundo M.,Hud, Nicholas V.

, p. 3504 - 3510 (2020/10/02)

Urea appears to be a key intermediate of important prebiotic synthetic pathways. Concentrated pools of urea likely existed on the surface of the early Earth, as urea is synthesized in significant quantities from hydrogen cyanide or cyanamide (widely accepted prebiotic molecules), it has extremely high water solubility, and it can concentrate to form eutectics from aqueous solutions. We propose a model for the origin of a variety of canonical and non-canonical nucleobases, including some known to form supramolecular assemblies that contain Watson-Crick-like base pairs.The dual nucleophilic-electrophilic character of urea makes it an ideal precursor for the formation of nitrogenous heterocycles. We propose a model for the origin of a variety of canonical and noncanonical nucleobases, including some known to form supramolecular assemblies that contain Watson-Crick-like base pairs. These reactions involve urea condensation with other prebiotic molecules (e. g., malonic acid) that could be driven by environmental cycles (e. g., freezing/thawing, drying/wetting). The resulting heterocycle assemblies are compatible with the formation of nucleosides and, possibly, the chemical evolution of molecular precursors to RNA. We show that urea eutectics at moderate temperature represent a robust prebiotic source of nitrogenous heterocycles. The simplicity of these pathways, and their independence from specific or rare geological events, support the idea of urea being of fundamental importance to the prebiotic chemistry that gave rise to life on Earth.

A compound and its preparation and use (by machine translation)

-

Paragraph 0091; 0092; 0093; 0095; 0102; 0104; 0111; 0113, (2018/03/25)

The present invention discloses a structure of the formula X compound or its pharmaceutically acceptable salt and its preparation and use: Wherein R1 is at least comprises a five-membered ring or a six-membered ring of chemical structure; R2 is a molecular weight greater than 100 and chemical structure containing electron-withdrawing group. (by machine translation)

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