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5-Benzylthio-1H-tetrazole - 0.25M in dry acetonitrile
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5-Benzylthio-1H-tetrazole - 0.25M in dry acetonitrile

CAS: 21871-47-6

Ref. 3D-FB156900

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Estimated delivery in United States, on Thursday 27 Jun 2024

Product Information

Name:
5-Benzylthio-1H-tetrazole - 0.25M in dry acetonitrile
Synonyms:
  • 5-Benzylmercapto-1H-tetrazoleBMTBTT
  • 1H-Tetrazole, 5-(benzylthio)-
  • 1H-Tetrazole, 5-[(phenylmethyl)thio]-
  • 2H-Tetrazole, 5-[(phenylmethyl)thio]-
  • 5-(benzylsulfanyl)-2H-tetrazole
  • 5-BenzyIthio-1H-Tetrazole
  • 5-Benzylmercapto-1,2,3,4-tetrazole
  • 5-Benzylmercapto-1H-Tetrazole
  • 5-Benzylmercaptotetrazole
  • 5-Benzylmercaptotetrazole (BMT)
  • See more synonyms
  • 5-Benzylthio-1H-Tetrazole (Btt)
  • 5-Benzylthio-1H-Tetrazole(Bmt)
  • 5-Benzylthiotetrazole
  • 5-Btt
  • 5-[((phenylmethyl)thio)thio]-1H-Tetrazole
  • 5-[(Phenylmethyl)Thio]-1H-Tetrazole
  • 5-[(Phenylmethyl)Thio]-1H-Tetrazole (Bmt)
  • 5-[(Phenylmethyl)thio]-2H-tetrazole
  • BMT
  • BTT
  • NSC 282041
  • Tetrazole, 5-(benzylthio)-
Description:

5-Benzylthio-1H-tetrazole is a monomer with high specificity, which can be immobilized on solid supports. It has been used in the synthesis of antiviral agents and bifunctional molecules. 5-Benzylthio-1H-tetrazole is a coreceptor antagonist that competes with HIV gp120 for binding to CD4, preventing the virus from entering CD4 cells. The molecule also inhibits the interaction between gp120 and cytidine deaminase, an enzyme that converts cytidine to uridine. This stepwise process inhibits the synthesis of viral DNA, leading to cell death by apoptosis.

Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
192.24 g/mol
Formula:
C8H8N4S
Purity:
Min. 98 Area-%
Color/Form:
Clear Liquid
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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