Benzo[d][1,2,3]thiadiazol-5-ylmethanol | CAS No. 615568-10-0

Benzo[d][1,2,3]thiadiazol-5-ylmethanol

Basic Information

CAS Number

615568-10-0

Molecular Formula

C7H6N2OS

Molecular Weight

166.21 g/mol

AD

Basic Physical Properties

C1=CC2=C(C=C1CO)N=NS2

InChI

InChI=1S/C7H6N2OS/c10-4-5-1-2-7-6(3-5)8-9-11-7/h1-3,10H,4H2

InChIKey

VCEGXPUFHUAMCE-UHFFFAOYSA-N

LogP

1.1836

Topological Polar Surface Area

46.010000000000005 Ų

Hydrogen Bond Donor/Acceptor

1 / 3

Complexity

144

Synonyms & References

English

  • Benzo[d][1,2,3]thiadiazol-5-ylmethanol
  • 1,2,3-Benzothiadiazol-5-ylmethanol
  • 1,2,3-Benzothiadiazole-5-methanol
  • VCEGXPUFHUAMCE-UHFFFAOYSA-N
  • A843317
  • benzothiadiazol-5-ylmethanol
  • DTXSID60619192
  • benzo[1,2,3]thiadiazol-5-yl-methanol
  • 615568-10-0
  • 1,2,3-BENZOTHIADIAZOL-5-YLMETHANOL
  • (1,2,3-Benzothiadiazol-5-yl)methanol
  • A843316
  • SCHEMBL3205606
  • benzo[d][1,2,3]thiadiazol-5-ylmethanol
  • DA-04398
  • J-519719

MDL Number

MFCD18909497

FAQ

What are the physical and chemical properties of Benzo[d][1,2,3]thiadiazol-5-ylmethanol (CAS: 615568-10-0)?

Benzo[d][1,2,3]thiadiazol-5-ylmethanol is a solid with a crystalline form. It has a molecular weight of approximately 216.26 g/mol and is poorly soluble in water but soluble in organic solvents like methanol and ethanol. It is reactive towards nucleophiles and can undergo substitution reactions. Its solubility and reactivity make it useful in various chemical processes.

How is Benzo[d][1,2,3]thiadiazol-5-ylmethanol (CAS: 615568-10-0) typically synthesized?

Benzo[d][1,2,3]thiadiazol-5-ylmethanol can be synthesized via the reaction of 5-(hydroxymethyl)benzimidazole with thiourea under basic conditions. The reaction involves the condensation of 5-(hydroxymethyl)benzimidazole with thiourea, followed by an acetylation step to protect the hydroxyl group. This method provides good yields and selectivity.

What industries use Benzo[d][1,2,3]thiadiazol-5-ylmethanol (CAS: 615568-10-0)?

Benzo[d][1,2,3]thiadiazol-5-ylmethanol is utilized in the pharmaceutical industry for its potential as a drug candidate, in polymer science for its cross-linking properties, and in sensor technology for its reactivity towards specific analytes. It is also explored in semiconductor manufacturing for its use as a precursor in thin film deposition processes.

What precautions should be taken when handling Benzo[d][1,2,3]thiadiazol-5-ylmethanol (CAS: 615568-10-0)?

When handling Benzo[d][1,2,3]thiadiazol-5-ylmethanol, it is important to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or a fume hood. Spills should be cleaned up immediately using appropriate safety measures, and the material safety data sheet (MSDS) should be consulted for detailed emergency procedures. It is also crucial to ensure proper storage in a cool, dry place away from direct sunlight and flammable materials.

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