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2-Mercaptobenzoxazole

  • CAS:2382-96-9
  • purity:99%
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Chinese Manufacturer supply 2-Mercaptobenzoxazole 2382-96-9 in stock with high standard

  • Molecular Formula: C7H5NOS
  • Molecular Weight: 151.189
  • Appearance/Colour: beige crystalline powder 
  • Vapor Pressure: 0.0258mmHg at 25°C 
  • Melting Point: 192-195 °C(lit.) 
  • Refractive Index: 1.714 
  • Boiling Point: 247.3 °C at 760 mmHg 
  • PKA: 11.03±0.20(Predicted) 
  • Flash Point: 103.4 °C 
  • PSA: 64.83000 
  • Density: 1.41 g/cm3 
  • LogP: 2.11650 

2-Mercaptobenzoxazole(Cas 2382-96-9) Usage

Preparation

2-Mercaptobenzoxazole has already been described in 1876 by Dunner (Ber. 9, (1876) page 465). 2-Mercaptobenzoxazole and its derivatives are prepared by processes which are based in principle on the reaction between o-aminophenol and alkali metal alkylxanthates. The alkali metal alkylxanthate here can either be employed as such, or it can be produced in the reaction mixture itself from an alkali, a lower alkanol and carbon disulphide.https://patents.google.com/patent/US4677209A/en

Reactions

2-Mercaptobenzoxazole with ethyl chloroacetate and anhydrous K2C03 in the presence of dry acetone was refluxed on water bath to give ethyl-2-(mercaptobenzoxazolo)acetate.

Application

2-Mercaptobenzoxazole is a widely used organic scaffold in medicinal chemistry.2-Mercaptobenzoxazole and their derivatives are known to posses several biological activities such as antibacterial, antifungal, antiinflammatory, insecticidal and herbicidal. 4-0xo-thiazolidines have also played an important activities as analgesic, anti-HIV, antitubercular, anthelmentic, dye-stuffs, fluorescent and as a photosensitizer. The incorporation of 4-oxothiazolidine and their 5-arylidene moieties in 2-mercaptobenzoxazole frame work has been found to enhance the activity.

InChI:InChI=1/C7H5NOS/c10-7-8-5-3-1-2-4-6(5)9-7/h1-4H,(H,8,10)

2382-96-9 Relevant articles

Photoaddition Reactions of Benzoxazole-2(3H)-thiones to Cycloalkenes and Heteroaromatics

Nishio, Takehiko,Shiwa, Kiyoko,Sakamoto, Masami

, p. 3255 - 3264 (2003)

Photoaddition reactions of benzoxazole-2...

Green synthesis of therapeutically active 1,3,4-oxadiazoles as antioxidants, selective COX-2 inhibitors and their in silico studies

Nesaragi, Aravind R.,Kamble, Ravindra R.,Dixit, Shruti,Kodasi, Barnabas,Hoolageri, Swati R.,Bayannavar, Praveen K.,Dasappa, Jagadeesh Prasad,Vootla, Shyamkumar,Joshi, Shrinivas D.,Kumbar, Vijay M.

supporting information, (2021/06/09)

A modest, competent and green synthetic ...

A green approach for the synthesis of benzazolyl pyrimidinyl carbamothioates under ultrasonication and their antimicrobial activity

Kayathi, Narendra Babu,Panga, Siva Sankar,Adivireddy, Padmaja,Venkatapuram, Padmavathi

, p. 2931 - 2943 (2021/07/26)

A library of benzazolyl pyrimidinyl carb...

Microwave facilitated one-pot three component synthesis of coumarin-benzoxazole clubbed 1,2,3-triazoles: Antimicrobial evaluation, molecular docking and in silico ADME studies

Nesaragi, Aravind R.,Kamble, Ravindra R.,Bayannavar, Praveen K.,Metre, Tukaram V.,Kariduraganavar, Mahadevappa Y.,Margankop, Sheetal B.,Joshi, Shrinivas D.,Kumbar, Vijay M.

, p. 3460 - 3472 (2021/10/02)

4-((4-((Benzo[d]oxazol-2-ylthio)methyl)-...

Synthesis, in?vitro biological screening and docking study of benzo[d]oxazole bis Schiff base derivatives as a potent anti-Alzheimer agent

Alhibshi, Amani H.,Anouar, El Hassane,Khan, Khalid Mohammed,Nawaz, Faisal,Rahim, Fazal,Rehman, Ashfaq Ur,Sajid, Muhammad,Shah, Adnan Ali,Taha, Muhammad,Uddin, Nizam,Wadood, Abdul,Zaman, Khalid

, (2022/01/14)

We have synthesized benzo[d]oxazole deri...

2382-96-9 Process route

piperidine
110-89-4

piperidine

2-thioxo-benzooxazole-3-carboximidic acid <i>p</i>-tolyl ester
70989-48-9

2-thioxo-benzooxazole-3-carboximidic acid p -tolyl ester

1-piperidinylcarbonnitrile
1530-87-6

1-piperidinylcarbonnitrile

benzo[d]oxazole-2-(3H)-thione
2382-96-9

benzo[d]oxazole-2-(3H)-thione

p-cresol
106-44-5

p-cresol

Conditions
Conditions Yield
In ethanol; for 0.5h; Heating;
87%
ethanol
64-17-5

ethanol

2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone
312313-33-0

2-phenyl-1-(2-thioxobenzo[d]oxazol-3(2H)-yl)ethanone

benzo[d]oxazole-2-(3H)-thione
2382-96-9

benzo[d]oxazole-2-(3H)-thione

Ethyl 2-phenylethanoate
101-97-3

Ethyl 2-phenylethanoate

Conditions
Conditions Yield
In chloroform-d1; at 20 ℃; for 5h; Irradiation;
95 % Spectr.
95 % Spectr.

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    ethanol

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