2-Amino-6-chloropyrimidine-4 (3H) -thione, English name: 2-amino-6-chloro-1H-pyrimidine-4-thione, CAS: 6310-02-7, chemical formula: C4H4ClN3S, molecular weight: 161.
6310-02-7
2-Amino-6-chloropyrimidine-4 (3H) -thione (2-amino-6-chloro-1H-pyrimidine-4-thione)
CAS: 6310-02-7
Chemical formula: C4H4ClN3S
<"" ="xl" "">| Chinese name | 2-Amino-6-chloropyrimidine-4 (3H) -thione |
| English name | 2-amino-6-chloro-1H-pyrimidine-4-thione |
| alias | 2-Amino-6-chloropyrimidine-4 (3H) -thione |
| English alias | 2-amino-6-chloro-1H-pyrimidine-4-thione 2-AMino-6-chloropyriMidine-4(3H)-thione 4(1H)-Pyrimidinethione, 2-amino-6-chloro- |
| CAS | 6310-02-7 |
| chemical formula | C4H4ClN3S |
| molecular weight | 161.61 |
| storage conditions | 2-8℃ |
6310-02-7 - brief introduction
2-Amino-6-chloropyrimidine-4 (3H) -thione, also known as 2-amino-6-chloro-1H-pyrimidine-4-thione, is an organosulfur compound. The following is a description of the properties, uses, preparation and safety information of this compound:Nature:
Appearance: 2-Amino-6-chloropyrimidine-4 (3H) -thione usually appears as white or yellowish crystals.
Solubility: Insoluble in water, but soluble in organic solvents such as ethanol, chloroform, and dimethyl ketone.
- Chemical properties: 2-Amino-6-chloropyrimidine-4 (3H) -thiones can form covalent bonds with guanine bases in DNA or RNA through the sulfur-checking point of nucleotides, thereby affecting nucleic acids.
Purpose:
Biological research: 2-Amino-6-chloropyrimidine-4 (3H) -thione is often used as a chemical reference for the detection of guanine bases in DNA or RNA.
Production method:
2-Amino-6-chloropyrimidine-4 (3H) -thiones can be synthesized by a variety of synthetic pathways, the most common method being the condensation reaction between pyrimidine iodide and the corresponding amino compound in the presence of sulfurous acid.
Safety information:
The toxicity and safety of 2-amino-6-chloropyrimidine-4 (3H) -thiones have not been reported in detail, and appropriate safety measures need to be taken when using or handling them.
Avoid inhalation, ingestion, or contact with skin.
Wear appropriate personal protective equipment during operation, such as laboratory gloves, protective glasses, and a laboratory jacket.
If you accidentally inhale or come into contact with the compound, seek medical attention immediately and show your doctor the packaging or chemical name of the compound.
When conducting chemical experiments or operations, relevant safe operating practices and established standard procedures shall be followed.Last Updated: 2024-04-09 20:49:11
