Welcome to LookChem.com Sign In|Join Free
  • or
6-amino-1,3-dimethyl-5-nitroso-2-thioxo-2,3-dihydropyrimidin-4(1H)-one is a complex organic compound belonging to the pyrimidine family. This molecule features a pyrimidine ring with a 6-amino group, two methyl groups at the 1 and 3 positions, a nitroso group at the 5 position, and a thioxo group at the 2 position. The compound is a 2,3-dihydro derivative, indicating the presence of two hydrogen atoms attached to the carbon atoms at positions 2 and 3. This chemical structure is significant in medicinal chemistry, as it can be a precursor or a building block for the synthesis of various biologically active molecules, including potential therapeutic agents. The specific arrangement of functional groups in 6-amino-1,3-dimethyl-5-nitroso-2-thioxo-2,3-dihydropyrimidin-4(1H)-one may confer unique chemical and biological properties, making it a subject of interest for further research and development in the field of drug discovery.

6501-95-7

Post Buying Request

6501-95-7 Suppliers

Recommended suppliers

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

6501-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6501-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6501-95:
(6*6)+(5*5)+(4*0)+(3*1)+(2*9)+(1*5)=87
87 % 10 = 7
So 6501-95-7 is a valid CAS Registry Number.

6501-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1,3-dimethyl-5-nitroso-2-sulfanylidenepyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-amino-1,3-dimethyl-5-nitroso-2-thiouracil

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:6501-95-7 SDS

6501-95-7Relevant academic research and scientific papers

Complexes with 6-amino-5-nitroso-2-thiouracil and violuric acid derivatives containing the fac-ReI(CO)3 core: Synthesis, XRD structural and photoluminescence characterization

Illán-Cabeza, Nuria A.,García-García, Antonio R.,Moreno-Carretero, Miguel N.

experimental part, p. 262 - 267 (2011/04/12)

The fac-tricarbonylrhenium(I) complexes of the 6-amino-1,3-dimethyl-5- nitroso-2-thiouracil (DANTU) and violuric acid (VIO) and its mono- (MVIO) and dimethyl (DVIO) derivatives have been prepared. The complexes have been characterized by elemental analysis, IR, 1H and 13C NMR spectral methods and luminescence spectroscopy. The structures of [ReCl(CO) 3(DANTU)], [Re(H2O)(CO)3(VIOH-1)] and [Re(H2O)(CO)3(DVIOH-1)] complexes were solved from single-crystal X-ray diffraction experiments. The coordination environment around the Re(I) may be described as a distorted octahedron in which the ligand behaves in a bidentate fashion through the nitrogen atom of the nitroso group and an adjacent carbonylic oxygen, making a five-membered chelate ring. The coordination sphere is completed with three carbonyl groups in fac-arrangement and one chlorine atom (DANTU complex) or water molecule (VIO complexes). The higher acidity of violuric acids, if compared with DANTU one, may explain both synergic deprotonation and chloride substitution in the [ReCl(CO)3]+ moiety to form the Re-violurato complexes.

Structure-Activity Relationships of 1,3-Dialkylxanthine Derivatives at Rat A3 Adenosine Receptors

Kim, Hea Ok,Ji, Xiao-duo,Melman, Neli,Olah, Mark E.,Stiles, Gary L.,Jacobson, Kenneth A.

, p. 3373 - 3382 (2007/10/02)

1,3-Dialkylxanthine analogues containing carboxylic acid and other charged groups on 8-position substituents were synthesized.These derivatives were examined for affinity in radioligand binding assays at rat brain A3 adenosine receptors stably

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6501-95-7