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CAS

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1606-76-4

2-Nitrothiazole, with the molecular formula C3H2N2O2S, is a yellow crystalline solid that serves as a key component in the synthesis of pharmaceuticals and other organic compounds. It is recognized for its antimicrobial properties and is being explored for its potential in treating bacterial and fungal infections. Moreover, it contributes to the production of dyes, pigments, and various industrial products. However, it is also classified as a potential mutagen and human carcinogen, necessitating stringent safety precautions during handling.

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  • 1606-76-4 Structure

  • Basic information

    1. Product Name: 2-Nitrothiazole
    2. Synonyms: 2-Nitrothiazole
    3. CAS NO:1606-76-4
    4. Molecular Formula: C3H2N2O2S
    5. Molecular Weight: 130.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1606-76-4.mol

  • Chemical Properties

    1. Melting Point: 76 °C
    2. Boiling Point: 278.6±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.549±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -1.83±0.10(Predicted)
    10. CAS DataBase Reference: 2-Nitrothiazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Nitrothiazole(1606-76-4)
    12. EPA Substance Registry System: 2-Nitrothiazole(1606-76-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1606-76-4(Hazardous Substances Data)

1606-76-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Nitrothiazole is used as a synthetic intermediate for the development of various pharmaceuticals, leveraging its antimicrobial properties to combat bacterial and fungal infections.
Used in Chemical Industry:
In the chemical industry, 2-Nitrothiazole is utilized as a building block in the production of dyes and pigments, contributing to the coloration and properties of these products.
Used in Industrial Product Manufacturing:
2-Nitrothiazole is employed in the manufacturing of other industrial products, where its chemical structure and properties are harnessed to enhance the performance of the final goods.

Check Digit Verification of cas no

The CAS Registry Mumber 1606-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1606-76:
(6*1)+(5*6)+(4*0)+(3*6)+(2*7)+(1*6)=74
74 % 10 = 4
So 1606-76-4 is a valid CAS Registry Number.

1606-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-1,3-thiazole

1.2 Other means of identification

Product number -
Other names ALNUOSXDMYFQNQ-UHFFFAOYSA

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:1606-76-4 SDS

1606-76-4Upstream product

1606-76-4Relevant articles and documents

Synthesis of dinitro-substituted furans, thiophenes, and azoles

Katritzky, Alan R.,Vakulenko, Anatoliy V.,Sivapackiam, Jothilingam,Draghici, Bogdan,Damavarapu, Reddy

, p. 699 - 706 (2008/09/21)

Direct nitration of the corresponding mononitro furans with fuming nitric acid, thiophenes with acetyl nitrate, and thiazoles with trifluoroacetyl nitrate, gave dinitro-substituted furans, thiophenes, and thiazoles. The nitrations of 2-alkylthiophenes wit

Non-fluorescent asymmetric cyanine dye compounds useful for quenching reporter dyes

-

, (2008/06/13)

The invention provides asymmetric cyanine dye compounds having the general formula: including substituted forms thereof, which are non-fluorescent quencher molecules. The invention further provides reporter-quencher dye pairs, wherein the asymmetric cyanine dyes are the quenchers, polynucleotides incorporating the asymmetric cyanine dyes, and nucleic acid hybridization detection methods utilizing the dye-labeled polynucleotides.

Nitro-substituted non-fluorescent asymmetric cyanine dye compounds

-

, (2008/06/13)

The invention provides an asymmetric cyanine dye compound having the structure including substituted forms thereof, wherein, at least one of R1 and R2 is linking group, X is O, S, or Se, and n ranges from 0 to 2. The invention further provides reporter-quencher dye pairs comprising the asymmetric cyanine dyes, dye-labeled polynucleotides incorporating the asymmetric cyanine dyes, and hybridization detection methods utilizing the dye-labeled polynucleotides.

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